A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040586



Internal ID21949929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:46834797..46834850hg38UCSC Ensembl
chr20:45463436..45463489hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633344
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040586
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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