A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17693065



Internal ID116731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:83891339..84087535hg38UCSC Ensembl
chr13:84465474..84661670hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38196197
hg19196197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5498162
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17693065
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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