A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17632495



Internal ID21824542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49023644..49023761hg38UCSC Ensembl
chr20:47640181..47640298hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6052531
Supporting Variants
Samples
Known GenesARFGEF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17632495
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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