This dataset contains counts of live births for California counties based on information entered on birth certificates. Final counts are derived from static data and include out of state births to California residents, whereas provisional counts are derived from incomplete and dynamic data. Provisional counts are based on the records available when the data was retrieved and may not represent all births that occurred during the time period.

The final data tables include both births that occurred in California regardless of the place of residence (by occurrence) and births to California residents (by residence), whereas the provisional data table only includes births that occurred in California regardless of the place of residence (by occurrence). The data are reported as totals, as well as stratified by parent giving birth's age, parent giving birth's race-ethnicity, and birth place type. See temporal coverage for more information on which strata are available for which years.

This dataset contains counts of live births for California as a whole based on information entered on birth certificates. Final counts are derived from static data and include out of state births to California residents, whereas provisional counts are derived from incomplete and dynamic data. Provisional counts are based on the records available when the data was retrieved and may not represent all births that occurred during the time period.

The final data tables include both births that occurred in California regardless of the place of residence (by occurrence) and births to California residents (by residence), whereas the provisional data table only includes births that occurred in California regardless of the place of residence (by occurrence). The data are reported as totals, as well as stratified by parent giving birth's age, parent giving birth's race-ethnicity, and birth place type. See temporal coverage for more information on which strata are available for which years.

Number and percentage of live births, by month of birth, 1991 to most recent year.

SELECTED SOCIAL CHARACTERISTICS IN THE UNITED STATES PLACE OF BIRTH - DP02 Universe - Total population Survey-Program - American Community Survey 5-year estimates Years - 2020, 2021, 2022 People not reporting a place of birth were assigned the state or country of birth of another family member, or were allocated the response of another individual with similar characteristics. People born outside the United States were asked to report their place of birth according to current international boundaries. Since numerous changes in boundaries of foreign countries have occurred in the last century, some people may have reported their place of birth in terms of boundaries that existed at the time of their birth or emigration, or in accordance with their own national preference.

This dataset of U.S. mortality trends since 1900 highlights the differences in age-adjusted death rates and life expectancy at birth by race and sex.

Age-adjusted death rates (deaths per 100,000) after 1998 are calculated based on the 2000 U.S. standard population. Populations used for computing death rates for 2011–2017 are postcensal estimates based on the 2010 census, estimated as of July 1, 2010. Rates for census years are based on populations enumerated in the corresponding censuses. Rates for noncensus years between 2000 and 2010 are revised using updated intercensal population estimates and may differ from rates previously published. Data on age-adjusted death rates prior to 1999 are taken from historical data (see References below).

Life expectancy data are available up to 2017. Due to changes in categories of race used in publications, data are not available for the black population consistently before 1968, and not at all before 1960. More information on historical data on age-adjusted death rates is available at https://www.cdc.gov/nchs/nvss/mortality/hist293.htm.

SOURCES

CDC/NCHS, National Vital Statistics System, historical data, 1900-1998 (see https://www.cdc.gov/nchs/nvss/mortality_historical_data.htm); CDC/NCHS, National Vital Statistics System, mortality data (see http://www.cdc.gov/nchs/deaths.htm); and CDC WONDER (see http://wonder.cdc.gov).

REFERENCES

1. National Center for Health Statistics, Data Warehouse. Comparability of cause-of-death between ICD revisions. 2008. Available from: http://www.cdc.gov/nchs/nvss/mortality/comparability_icd.htm.

2. National Center for Health Statistics. Vital statistics data available. Mortality multiple cause files. Hyattsville, MD: National Center for Health Statistics. Available from: https://www.cdc.gov/nchs/data_access/vitalstatsonline.htm.

3. Kochanek KD, Murphy SL, Xu JQ, Arias E. Deaths: Final data for 2017. National Vital Statistics Reports; vol 68 no 9. Hyattsville, MD: National Center for Health Statistics. 2019. Available from: https://www.cdc.gov/nchs/data/nvsr/nvsr68/nvsr68_09-508.pdf.

4. Arias E, Xu JQ. United States life tables, 2017. National Vital Statistics Reports; vol 68 no 7. Hyattsville, MD: National Center for Health Statistics. 2019. Available from: https://www.cdc.gov/nchs/data/nvsr/nvsr68/nvsr68_07-508.pdf.

5. National Center for Health Statistics. Historical Data, 1900-1998. 2009. Available from: https://www.cdc.gov/nchs/nvss/mortality_historical_data.htm.

The Stockholm Birth Cohort Study (SBC) was created in 2004/2005 by a probability matching of two anonymized longitudinal datasets; The Stockholm Metropolitan study and The Swedish Work and Mortality Database (WMD). The former involves all children born 1953 that lived in the Stockholm metropolitan area as of November 1, 1963, while the latter comprises data for the period 1980-2009 on all individuals living in Sweden in 1980 or 1990, and born before 1986.

The study comprises data from both surveys and public register records. The core of the project consists of three surveys from The Stockholm Metropolitan study; The School Study (1966), The Family Study (1968), and The Culture and Leisure Time Study (1985). There is also a wide range of register data, for instance delivery records, occupational and income data, welfare recipiency data, health records, mortality data, educational data, and dependency and child welfare committee data.

The Stockholm Birth Cohort offers unique opportunities for longitudinal research within various fields such as sociology, public health science, and psychology. So far the datasets have resulted in more than 140 publications which have dealt with, among other things, whether and how childhood circumstances affect later social outcomes in adult life.

Purpose:

To aim is to create a new tool for life-course studies of health outcomes as well as social outcomes for research in fields such as psychology, public health science, and sociology.

Yearly registered births – breakdown by Month

The National Child Development Study (NCDS) is a continuing longitudinal study that seeks to follow the lives of all those living in Great Britain who were born in one particular week in 1958. The aim of the study is to improve understanding of the factors affecting human development over the whole lifespan.

The NCDS has its origins in the Perinatal Mortality Survey (PMS) (the original PMS study is held at the UK Data Archive under SN 2137). This study was sponsored by the National Birthday Trust Fund and designed to examine the social and obstetric factors associated with stillbirth and death in early infancy among the 17,000 children born in England, Scotland and Wales in that one week. Selected data from the PMS form NCDS sweep 0, held alongside NCDS sweeps 1-3, under SN 5565.

Survey and Biomeasures Data (GN 33004):
To date there have been nine attempts to trace all members of the birth cohort in order to monitor their physical, educational and social development. The first three sweeps were carried out by the National Children's Bureau, in 1965, when respondents were aged 7, in 1969, aged 11, and in 1974, aged 16 (these sweeps form NCDS1-3, held together with NCDS0 under SN 5565). The fourth sweep, also carried out by the National Children's Bureau, was conducted in 1981, when respondents were aged 23 (held under SN 5566). In 1985 the NCDS moved to the Social Statistics Research Unit (SSRU) - now known as the Centre for Longitudinal Studies (CLS). The fifth sweep was carried out in 1991, when respondents were aged 33 (held under SN 5567). For the sixth sweep, conducted in 1999-2000, when respondents were aged 42 (NCDS6, held under SN 5578), fieldwork was combined with the 1999-2000 wave of the 1970 Birth Cohort Study (BCS70), which was also conducted by CLS (and held under GN 33229). The seventh sweep was conducted in 2004-2005 when the respondents were aged 46 (held under SN 5579), the eighth sweep was conducted in 2008-2009 when respondents were aged 50 (held under SN 6137) and the ninth sweep was conducted in 2013 when respondents were aged 55 (held under SN 7669).

Four separate datasets covering responses to NCDS over all sweeps are available. National Child Development Deaths Dataset: Special Licence Access (SN 7717) covers deaths; National Child Development Study Response and Outcomes Dataset (SN 5560) covers all other responses and outcomes; National Child Development Study: Partnership Histories (SN 6940) includes data on live-in relationships; and National Child Development Study: Activity Histories (SN 6942) covers work and non-work activities. Users are advised to order these studies alongside the other waves of NCDS.

From 2002-2004, a Biomedical Survey was completed and is available under End User Licence (EUL) (SN 8731) and Special Licence (SL) (SN 5594). Proteomics analyses of blood samples are available under SL SN 9254.

Linked Geographical Data (GN 33497):
A number of geographical variables are available, under more restrictive access conditions, which can be linked to the NCDS EUL and SL access studies.

Linked Administrative Data (GN 33396):
A number of linked administrative datasets are available, under more restrictive access conditions, which can be linked to the NCDS EUL and SL access studies. These include a Deaths dataset (SN 7717) available under SL and the Linked Health Administrative Datasets (SN 8697) available under Secure Access.

Additional Sub-Studies (GN 33562):
In addition to the main NCDS sweeps, further studies have also been conducted on a range of subjects such as parent migration, unemployment, behavioural studies and respondent essays. The full list of NCDS studies available from the UK Data Service can be found on the NCDS series access data webpage.

How to access genetic and/or bio-medical sample data from a range of longitudinal surveys:
For information on how to access biomedical data from NCDS that are not held at the UKDS, see the CLS Genetic data and biological samples webpage.

Further information about the full NCDS series can be found on the Centre for Longitudinal Studies website.
The National Child Development Deaths Dataset, 1958-2014: Special Licence Access contains data on known deaths among members of the NCDS birth cohort from 1958 to 2013. Information on deaths has been taken from the records maintained by the organisations responsible for the study over the life time of the study: the National Birthday Trust Fund, the National Children’s Bureau (NCB), the Social Statistics Research Unit (SSRU) and the CLS. The information has been gleaned from a variety of sources, including death certificates and other information from the National Health Service Central Register (NHSCR), and from relatives and friends during survey activities and cohort maintenance work by telephone, letter and e-mail. It includes all deaths up to 31st December 2013. In only 6 cases are the date of death unknown. By the end of December 8.7 per cent of the cohort were known to have died.

The National Child Development Study Response and Outcomes Dataset, 1958-2013 (SN 5560) covers other responses and outcomes of the cohort members and should be used alongside this dataset.

For the 3rd edition (July 2018) an updated version of the data was deposited. The new edition includes data on known deaths among members of the National Child Development Study (NCDS) birth cohort up to 2016. The user guide has also been updated.

The census is undertaken by the Office for National Statistics every 10 years and gives us a picture of all the people and households in England and Wales. The most recent census took place in March of 2021.The census asks every household questions about the people who live there and the type of home they live in. In doing so, it helps to build a detailed snapshot of society. Information from the census helps the government and local authorities to plan and fund local services, such as education, doctors' surgeries and roads.Key census statistics for Leicester are published on the open data platform to make information accessible to local services, voluntary and community groups, and residents. There is also a dashboard published showcasing various datasets from the census allowing users to view data for the MSOAs of Leicester and compare this with Leicester overall statistics.Further information about the census and full datasets can be found on the ONS website - https://www.ons.gov.uk/census/aboutcensus/censusproductsCountry of birthThis dataset provides Census 2021 estimates that classify usual residents in England and Wales by their country of birth. The estimates are as at Census Day, 21 March 2021.Definition: The country in which a person was born. For people not born in one of in the four parts of the UK, there was an option to select "elsewhere". People who selected "elsewhere" were asked to write in the current name for their country of birth.

Births that occurred by hospital name. Birth events of 5 or more per hospital location are displayed

This is a publication on maternity activity in English NHS hospitals. This report examines data relating to delivery and birth episodes in 2021-22, and the booking appointments for these deliveries. This annual publication covers the financial year ending March 2022. Data is included from both the Hospital Episodes Statistics (HES) data warehouse and the Maternity Services Data Set (MSDS). HES contains records of all admissions, appointments and attendances for patients admitted to NHS hospitals in England. The HES data used in this publication are called 'delivery episodes'. The MSDS collects records of each stage of the maternity service care pathway in NHS-funded maternity services, and includes information not recorded in HES. The MSDS is a maturing, national-level dataset. In April 2019 the MSDS transitioned to a new version of the dataset. This version, MSDS v2.0, is an update that introduced a new structure and content - including clinical terminology, in order to meet current clinical practice and incorporate new requirements. It is designed to meet requirements that resulted from the National Maternity Review, which led to the publication of the Better Births report in February 2016. This is the third publication of data from MSDS v2.0 and data from 2019-20 onwards is not directly comparable to data from previous years. This publication shows the number of HES delivery episodes during the period, with a number of breakdowns including by method of onset of labour, delivery method and place of delivery. It also shows the number of MSDS deliveries recorded during the period, with breakdowns including the baby's first feed type, birthweight, place of birth, and breastfeeding activity; and the mothers' ethnicity and age at booking. There is also data available in a separate file on breastfeeding at 6 to 8 weeks. The count of Total Babies includes both live and still births, and previous changes to how Total Babies and Total Deliveries were calculated means that comparisons between 2019-20 MSDS data and later years should be made with care. The MethodfDelivery measure counting babies has been replaced by the DeliveryMethodBabyGroup measure which counts deliveries, and the smoking at booking and folic acid status measures have been renamed - these changes have been made to better align this annual publication with the Maternity Services Monthly Statistics publication. Information on how all measures are constructed can be found in the HES Metadata and MSDS Metadata files provided below. In this publication we have also included an interactive Power BI dashboard to enable users to explore key NHS Maternity Statistics measures. The purpose of this publication is to inform and support strategic and policy-led processes for the benefit of patient care. This report will also be of interest to researchers, journalists and members of the public interested in NHS hospital activity in England. Any feedback on this publication or dashboard can be provided to enquiries@nhsdigital.nhs.uk, under the subject “NHS Maternity Statistics”.

This data set lists the sex and number of birth registrations for each first name, from 1900 onward. Years are grouped by the date of the birth registration, not by the date of birth. Some birth registrations are not included, such as registrations with a sex other than Male or Female (i.e. indeterminate or not recorded), or where the birth registration date is not recorded. These excluded records are so few their exclusion is unlikely to have any significant impact on the data. Where a name has less than 10 instances in a particular year, the name will not be included in the data for that year. Due to this, total volumes will be less than the total birth registrations in that year. As first and middle names are recorded in our system together, the first name has been split off from the middle names. Due to the size of the data set, this was done with an automated system, generally looking for the first space in the name. This means there may be names not correctly added. Also, certain symbols in names may not carry through to the data correctly. Please let us know using the contact email address if you find any errors in the data.

Number and percentage of live births, by marital status of mother, 1991 to most recent year.

California Birth Report totals by Birth Characteristics to inform the public, stakeholders, and researchers.

The DHCS Medi-Cal Birth Statistics tables present the descriptive statistics for California resident births that occurred in a hospital setting, including data on maternal characteristics, delivery methods, and select birth outcomes such as low birthweight and preterm delivery. Tables also include key comorbidities and health behaviors known to influence birth outcomes, such as hypertension, diabetes, substance use, pre-pregnancy weight, and smoking during pregnancy.

DHCS additionally presents birth statistics for women participating in the Medi-Cal Fee-For-Service (FFS) and managed care delivery systems, as well as births financed by private insurance, births financed by other public funding sources, and births among uninsured mothers. Medi-Cal data reflect mothers that were deemed as Medi-Cal certified eligible.

Note: Data for maternal comorbidities including hypertension, diabetes, and substance use have been provisionally omitted among calendar years 2020-2022 for the time being.

This dataset provides Census 2021 estimates that classify usual residents in England and Wales by their country of birth, this dataset comprises a more detailed breakdown of birth country. The estimates are as at Census Day, 21 March 2021.

Census 2021 rounded migration estimates for local authorities in England and Wales were originally released on 28 June 2022 in rounded form. The bulletin explored change over time, regional variations and the composition of the population by sex and by five-year age group.

This update provides unrounded migration estimates from Country level down to Output Area.

Area type

Census 2021 statistics are published for a number of different geographies. These can be large, for example the whole of England, or small, for example an output area (OA), the lowest level of geography for which statistics are produced.

For higher levels of geography, more detailed statistics can be produced. When a lower level of geography is used, such as output areas (which have a minimum of 100 persons), the statistics produced have less detail. This is to protect the confidentiality of people and ensure that individuals or their characteristics cannot be identified.

Coverage

Census 2021 statistics are published for the whole of England and Wales. Data are also available in these geographic types:

• country - for example, Wales
• region - for example, London
• local authority - for example, Cornwall
• health area – for example, Clinical Commissioning Group
• statistical area - for example, MSOA or LSOA

Country of birth

The country in which a person was born.

For people not born in one of in the four parts of the UK, there was an option to select "elsewhere".

People who selected "elsewhere" were asked to write in the current name for their country of birth.

This dataset as reported to the Rural Payments Agency contains cattle passport applications received for live animals, cattle born in Great Britain, applications received by all sources (Cattle Tracing System Online, Cattle Tracing System web services, standard interface system email, paper)

This dataset describes birth outcomes (weight, gestational age, sex assigned at birth, presence of birth defects, etc.) and parental factors (age, address, health status, etc.) for people born in North Carolina between 2003 and 2015. This dataset is not publicly accessible because: EPA cannot release personally identifiable information regarding living individuals, according to the Privacy Act and the Freedom of Information Act (FOIA). This dataset contains information about human research subjects. Because there is potential to identify individual participants and disclose personal information, either alone or in combination with other datasets, individual level data are not appropriate to post for public access. Restricted access may be granted to authorized persons by contacting the party listed. It can be accessed through the following means: Data come from the North Carolina Birth Defects Monitoring Program. These data are not publicly available, but more information can be obtained at https://schs.dph.ncdhhs.gov/units/bdmp/ (accessed 11/9/2021). Format: Data are stored as csv files and contain information on birth records in North Carolina from 2003 to 2015, including addresses of parents and medical information on parents and neonates.

This dataset is associated with the following publication: Slawsky, E., A. Weaver, T. Luben, and K. Rappazzo. A Cross-sectional Study of Brownfields and Birth Defects. Birth Defects Research. John Wiley & Sons, Inc., Hoboken, NJ, USA, 114(5-6): 197-207, (2022).

The data (name, year of birth, sex, and number) are from a 100 percent sample of Social Security card applications for 1880 onward.

Estimated annual number of births by gender for Canada, provinces and territories.