Article

dbVar structural variant cluster set for data analysis and variant comparison

2017-02-28

Abstract excerpt

dbVar houses over 3 million submitted structural variants (SSV) from 120 human studies including copy number variations (CNV), insertions, deletions, inversions, translocations, and complex chromosomal rearrangements. Users can submit multiple SSVs to dbVAR that are presumably identical, but were ascertained by different platforms and samples, to calculate whether the variant is rare or common in the population...

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Literature Corpus work: 3f7ff75b-dd46-519d-8d5b-5ecd4781cd48
DOI: 10.12688/f1000research.8290.2

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