A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17019071



Internal ID80341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:10822000..11260000hg38UCSC Ensembl
chr9:10822000..11260000hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38438001
hg19438001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142712
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17019071
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000313


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