A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702861



Internal ID126527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63331257..63331334hg38UCSC Ensembl
chr15:63623456..63623533hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5527354
Supporting Variants
Samples
Known GenesCA12
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702861
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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