A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17052296



Internal ID102713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119981266..119981447hg38UCSC Ensembl
chr11:119851975..119852156hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5502193
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17052296
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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