A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17047293



Internal ID99372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45720364..45720561hg38UCSC Ensembl
chr11:45741914..45742111hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5500023
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17047293
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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