A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17727394



Internal ID151060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11458083..11461202hg38UCSC Ensembl
chrUn_gl000233:30027..33146hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383120
hg193120
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5538162
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17727394
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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