A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16917604



Internal ID12477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:119525206..119525569hg38UCSC Ensembl
chr2:120282782..120283145hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg38364
hg19364
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5447943
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16917604
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.405017


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