A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059432



Internal ID21968665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32046912..32050490hg38UCSC Ensembl
chr20:30634715..30638293hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg383579
hg193579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628440
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059432
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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