A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17731666



Internal ID155332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24168773..24172964hg38UCSC Ensembl
chr20:24149409..24153600hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg384192
hg194192
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5530155
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17731666
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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