A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728621



Internal ID152287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33795381..33797706hg38UCSC Ensembl
chr22:34191368..34193693hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg382326
hg192326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5540792
Supporting Variants
Samples
Known GenesLARGE
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728621
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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