A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115666



Internal ID21298932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:80175624..80287223hg38UCSC Ensembl
Innerchr6:80885341..80996940hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38111600
hg19111600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14084483
Samplessample97
Known GenesBCKDHB
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115666
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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