A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17620012



Internal ID21812059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:7916914..7926421hg38UCSC Ensembl
chr20:7897561..7907068hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg389508
hg199508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6049658
Supporting Variants
Samples
Known GenesHAO1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17620012
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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