A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16932236



Internal ID22214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37362476..37363018hg38UCSC Ensembl
chr3:37403967..37404509hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38543
hg19543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5447039
Supporting Variants
Samples
Known GenesGOLGA4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16932236
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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