A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732258



Internal ID155924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37305007..37305999hg38UCSC Ensembl
chr20:35933410..35934402hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38993
hg19993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5526683
Supporting Variants
Samples
Known GenesMANBAL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732258
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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