A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043615



Internal ID21952909
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 StatusM
Merged Variants
Supporting Variantsnssv17632159
Samples
Known GenesRALGAPA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043615
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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