These tracks help you compare case findings against internal and public population data.
[Organization DB] tracks display variants from organization databases.
Left-click a variant to review variant details from the database:
Allele frequency
Allele count and allele number
Heterozygote and homozygote or hemizygote counts
Sample IDs where the variant was last observed
The gnomAD SV track displays structural variants from gnomAD.
Use it to review population frequency and distribution across diverse cohorts to support clinical relevance assessment.
The DGV Gold track displays high-confidence structural variants curated by the Database of Genomic Variants.
Use it as a reference for common benign structural variants.
The Decipher Healthy Population track displays variants observed in healthy individuals from the Deciphering Developmental Disorders study.
Use it to compare findings against a baseline of unaffected genomes.
Last updated 14 days ago
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