A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052531



Internal ID21961764
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 StatusM
Merged Variants
Supporting Variantsnssv17632495
Samples
Known GenesARFGEF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052531
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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