A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16939874



Internal ID27308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:131741540..131781865hg38UCSC Ensembl
chr3:131460384..131500709hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3840326
hg1940326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438595
Supporting Variants
Samples
Known GenesCPNE4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16939874
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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