dbVar

dbVar is NCBI's database of human genomic structural variation — insertions, deletions, duplications, inversions, mobile elements, translocations, and others

Getting Started

Overview of Structural Variation
Organism List
FAQ
Help
Factsheet

Accessing Data

Structural Variation Data Hub
Tools for analyzing dbVar data
Study Browser
Genome Browser
FTP Data Download

Other NCBI Resources

dbSNP
ClinVar
Variation Portal
Variation Tools

Non-Redundant Structural Variation Datasets

Would you like to compare and analyze your data with known structural variants (SV) in dbVar? Now there are easy-to-use files containing non-redundant (NR) deletions, duplications, and insertions aggregated from across studies in dbVar. The files are available for human assembly versions GRCh37 and GRCh38. Descriptions of the NR data and tutorials are available on GitHub.