A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17693108



Internal ID116774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:72319467..72370648hg38UCSC Ensembl
chr13:72893605..72944786hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3851182
hg1951182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5511063
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17693108
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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