Personal%20Genome%20Variants%20%28Blue%3AGain%3BRed%3ALoss%3BBrown%3AComplex%3BPurple%3AInversion%3BBlack%3AUnknown%29

This track shows the location of insertion/deletion variants detected in personal genome sequencing projects. Variants included here represent those which were detected in studies that are represented in DGV, but which were already submitted and accessioned in dbSNP. To avoid assigning multiple accessions to the same variants, these have been provided as a separate dataset. Last Update: 2012/01/31