A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023465



Internal ID83362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32714000..32733500hg38UCSC Ensembl
chr9:32713998..32733498hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3819501
hg1919501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5477213
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023465
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000937


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