A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728953



Internal ID152619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38663420..38663746hg38UCSC Ensembl
chr22:39059425..39059751hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5535173
Supporting Variants
Samples
Known GenesCBY1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728953
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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