A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17731982



Internal ID155648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32764047..32764146hg38UCSC Ensembl
chr20:31351853..31351952hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521032
Supporting Variants
Samples
Known GenesDNMT3B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17731982
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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