A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023462



Internal ID83359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32684457..32684524hg38UCSC Ensembl
chr9:32684455..32684522hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483546
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023462
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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