A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024229



Internal ID83891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67847387..67917387hg38UCSC Ensembl
chr9:44060387..44130447hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3870001
hg1970061
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142357
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024229
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.006222


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