A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17583782



Internal ID21775825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:22183183..22183274hg38UCSC Ensembl
chr9:22183182..22183273hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6004538
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17583782
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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