A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732327



Internal ID155993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38781694..38792686hg38UCSC Ensembl
chr20:37410337..37421329hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3810993
hg1910993
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522035
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732327
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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