A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738468



Internal ID162134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66591387..66713846hg38UCSC Ensembl
chr9:41808145..41930502hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38122460
hg19122358
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141912
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738468
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003125


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