A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16929191



Internal ID20167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16280773..16283237hg38UCSC Ensembl
chr3:16322280..16324744hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg382465
hg192465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5445408
Supporting Variants
Samples
Known GenesOXNAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16929191
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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