A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016434



Internal ID21925777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:20786159..20800997hg38UCSC Ensembl
chr8:20643670..20658508hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3814839
hg1914839
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576659
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016434
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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