We are happy to release the dbVar composite tracks, providing a curated resource for structural variant datasets on human GRCh37/hg19 and GRCh38/hg38 genome assemblies. The track aggregates data from more than one hundred sources including Gnomad, 1000 Genomes Consortium, and Decipher from the dbVar, the database of Structural Variation from NCBI. -The Common Stuctural Variants track shows variants that meet the following criteria: +The Common Structural Variants track shows variants that meet the following criteria: more than 50 basepairs, occur in at least 100 samples, and have an allele frequency of >=0.01 in at least one population. For more information, please see the track description page:
We thank the dbVar team at NCBI, especially John Lopez and Tim Hefferon for technical coordination and consultation, and to Chris Lee, Anna Benet-Pages, and Daniel Schmelter of the Genome Browser team for developing, and releasing this track.