A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728526



Internal ID152192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31946075..31946346hg38UCSC Ensembl
chr22:32342061..32342332hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5549079
Supporting Variants
Samples
Known GenesYWHAH
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728526
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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