A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028016



Internal ID86372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126294622..126294675hg38UCSC Ensembl
chr9:129056901..129056954hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5490297
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028016
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.013281


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