A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732051



Internal ID155717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33831745..33831782hg38UCSC Ensembl
chr20:32419551..32419588hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5536419
Supporting Variants
Samples
Known GenesCHMP4B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732051
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001093


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