A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17694078



Internal ID117744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97756774..97791313hg38UCSC Ensembl
chr13:98409028..98443567hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3834540
hg1934540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5499041
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17694078
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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