A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17022386



Internal ID82605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:20101582..20106896hg38UCSC Ensembl
chr9:20101580..20106894hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg385315
hg195315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486722
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17022386
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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