A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17632159



Internal ID21824206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20659296..20661790hg38UCSC Ensembl
chr20:20639940..20642434hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg382495
hg192495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6043615
Supporting Variants
Samples
Known GenesRALGAPA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17632159
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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