A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728937



Internal ID152603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38509222..38512880hg38UCSC Ensembl
chr22:38905227..38908885hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg383659
hg193659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5539773
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728937
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001561


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