A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732692



Internal ID156358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:46787646..46788633hg38UCSC Ensembl
chr20:45416285..45417272hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38988
hg19988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531660
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732692
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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