A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113427



Internal ID21296693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:46911213..47042039hg38UCSC Ensembl
Innerchr1:47376885..47507711hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38130827
hg19130827
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14082939
Samplessample172
Known GenesCYP4A11, CYP4X1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113427
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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