A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17691590



Internal ID115256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:63817183..65941383hg38UCSC Ensembl
chr13:64391316..66515515hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg382124201
hg192124200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5502560
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17691590
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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