A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728977



Internal ID152643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39030132..39050500hg38UCSC Ensembl
chr22:39426137..39446505hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3820369
hg1920369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5551582
Supporting Variants
Samples
Known GenesAPOBEC3D, APOBEC3F
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728977
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00047


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