A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113666



Internal ID21296932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:6599389..6629728hg38UCSC Ensembl
Innerchr1:6659449..6689788hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg3830340
hg1930340
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14099130
Samplessample360
Known GenesKLHL21, PHF13, THAP3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113666
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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