A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17692100



Internal ID115766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:66142106..66228106hg38UCSC Ensembl
chr13:66716238..66802238hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3886001
hg1986001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143190
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17692100
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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