A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023056



Internal ID83080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62497738..62678500hg38UCSC Ensembl
chr9:46809039..46989801hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38180763
hg19180763
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141618
Supporting Variants
Samples
Known GenesLOC643648
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023056
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.026622


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