A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728717



Internal ID152383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35596763..35597531hg38UCSC Ensembl
chr22:35992810..35993578hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38769
hg19769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5539048
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728717
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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