A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728908



Internal ID152574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38189069..38189176hg38UCSC Ensembl
chr22:38585076..38585183hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146666
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728908
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.178488


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