A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111474



Internal ID21294740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:93181974..93203816hg38UCSC Ensembl
Innerchr6:93891692..93913534hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3821843
hg1921843
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14082791
Samplessample1
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111474
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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