A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17059071



Internal ID107250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62935000..62958000hg38UCSC Ensembl
chr9:66590824..66613824hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3823001
hg1923001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142267
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17059071
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003779


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