A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023494



Internal ID83382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33015520..33023809hg38UCSC Ensembl
chr9:33015518..33023807hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg388290
hg198290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485359
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023494
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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