A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728979



Internal ID152645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39035564..39063782hg38UCSC Ensembl
chr22:39431569..39459787hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3828219
hg1928219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5536678
Supporting Variants
Samples
Known GenesAPOBEC3F
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728979
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000315


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