A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045802



Internal ID21955060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:48935988..48936162hg38UCSC Ensembl
chr20:47552525..47552699hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633548
Samples
Known GenesARFGEF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045802
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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