Database Commons
Database Commons

a catalog of worldwide biological databases

Database Profile

database of abnormal CVS cases

General information

URL: http://www.ncl.ac.uk/cvs
Full name:
Description: Following detection of a cytogenetic abnormality during prenatal diagnosis using CVS, use of this database allows rapid access to comparable cases from the United Kingdom and the literature. This database will improve the speed of availability and quality of information available to clinicians and patients for pregnancy management and counselling purposes.
Year founded: 2006
Last update:
Version:
Accessibility:
Unaccessible
Country/Region: United Kingdom

Contact information

University/Institution: Institute of Human Genetics
Address: Cytogenetic Laboratory, Northern Genetics Service, Institute of Human Genetics, Central Parkway, Newcastle upon Tyne, NE1 3BZ, UK
City: Newcastle
Province/State:
Country/Region: United Kingdom
Contact name (PI/Team): Wolstenholme J
Contact email (PI/Helpdesk): john.wolstenhome@ncl.ac.uk

Publications

16532524
Association of Clinical Cytogeneticists chorion villus sampling database 1987-2000. [PMID: 16532524]
Wolstenholme J, Emslie JB, Connors S.

OBJECTIVES: To produce a fully searchable Microsoft Access database of mosaic and non-mosaic cytogenetic abnormalities, detected during diagnostic chorionic villi sampling (CVS) to aid laboratories in predicting pregnancy outcome, in particular differentiating between cases of likely genuine fetal cytogenetic abnormalities and those likely to represent confined placental mosaicism (CPM).
METHODS: Retrospective collection of referral data, initial karyotype data, follow-up karyotype data and pregnancy outcome data from almost all cytogenetically abnormal diagnostic CVS, processed in UK National Health Service laboratories, between 1987 and 2000. Collection of similar data from a published series of CVS and individual case reports.
RESULTS: A fully searchable database of abnormal CVS cases, containing over 5000 entries, has been produced. This is available to download at http://www.ncl.ac.uk/cvs/.
CONCLUSIONS: Following detection of a cytogenetic abnormality during prenatal diagnosis using CVS, use of this database allows rapid access to comparable cases from the United Kingdom and the literature. This database will improve the speed of availability and quality of information available to clinicians and patients for pregnancy management and counselling purposes. The database has been designed with future data collection in mind, and can be developed for wider research use, through more detailed registries of individual chromosome abnormalities.

Prenat Diagn. 2006:26(5) | 3 Citations (from Europe PMC, 2025-12-13)

Ranking

All databases:
6714/6895 (2.64%)
Genotype phenotype and variation:
975/1005 (3.085%)
6714
Total Rank
3
Citations
0.158
z-index

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Record metadata

Created on: 2018-02-08
Curated by:
Meiye Jiang [2018-02-24]
Pei Wang [2018-02-08]