databases > DOI:10.25504/FAIRsharing.ktafj3

ready Database of genomic structural VARiation


General Information
dbVar is a database of genomic structural variation. It accepts data from all species and includes clinical data. It can accept diverse types of events, including inversions, insertions and translocations. Additionally, both germline and somatic variants are accepted.

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Countries that developed this resource United States

Created in 2010

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How to cite this record dbVar; Database of genomic structural VARiation; DOI:; Last edited: Jan. 8, 2019, 1:19 p.m.; Last accessed: Nov 29 2020 1:12 a.m.

This record is maintained by dbSNP

Record updated: Aug. 1, 2016, 2:54 p.m. by The FAIRsharing Team.

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DbVar and DGVa: public archives for genomic structural variation.

Lappalainen I., Lopez J., Skipper L., Hefferon T., Spalding JD., Garner J., Chen C., Maguire M., Corbett M., Zhou G., Paschall J., Ananiev V., Flicek P., Church DM.,
Nucleic Acids Res. 2013

View Paper (PubMed) View Publication

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  • This record is maintained by dbSNP