A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732697



Internal ID156363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:46819832..46829498hg38UCSC Ensembl
chr20:45448471..45458137hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg389667
hg199667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520990
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732697
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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