A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732119



Internal ID155785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34676880..34677076hg38UCSC Ensembl
chr20:33264684..33264880hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5526188
Supporting Variants
Samples
Known GenesPIGU
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732119
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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