A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931461



Internal ID21718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32112248..32112360hg38UCSC Ensembl
chr3:32153740..32153852hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5445169
Supporting Variants
Samples
Known GenesGPD1L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931461
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.485326


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