A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17691767



Internal ID115433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:68913443..68914173hg38UCSC Ensembl
chr13:69487575..69488305hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5496546
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17691767
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001405


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