A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728376



Internal ID152042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:29591698..29602171hg38UCSC Ensembl
chr22:29987687..29998160hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3810474
hg1910474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5534496
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728376
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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