A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704018



Internal ID127684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81568292..81917182hg38UCSC Ensembl
chr15:81860633..82209523hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38348891
hg19348891
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531904
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704018
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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