A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043169



Internal ID96487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5476752..5477271hg38UCSC Ensembl
chr11:5497982..5498501hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38520
hg19520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5505428
Supporting Variants
Samples
Known GenesOR51B5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043169
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00281


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