Description

The tracks listed here contain structural variants using long-read sequencing technologies.

• CoLoRSdb Small variants: small genetic variants (single nucleotide polymorphisms and short insertions and deletions) called with DeepVariant and merged with GLnexus/bcftools.
• CoLoRdb Structural variants: structural variants (insertions, deletions, and inversions) discovered with pbsv and merged across samples using Jasmine.

Display conventions

Hover over the feature to see more information, explained on teh track details page of the particular track or when clicking onto the feature.

Credits

For data provenance, access and descriptions, please click the documentation via the link above.