databases > DOI:10.25504/FAIRsharing.ktafj3

ready Database of genomic structural VARiation

Abbreviation:dbVar

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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.


This record replaces or incorporates the following deprecated resources:

Homepage http://www.ncbi.nlm.nih.gov/dbvar/

Countries that developed this resource United States

Created in 2010

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How to cite this record FAIRsharing.org: dbVar; Database of genomic structural VARiation; DOI: https://doi.org/10.25504/FAIRsharing.ktafj3; Last edited: Jan. 8, 2019, 1:19 p.m.; Last accessed: Sep 20 2019 12:38 p.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

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  • This record is maintained by dbSNP

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