A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115712



Internal ID21298978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48204753..48215352hg38UCSC Ensembl
Innerchr14:48673956..48684555hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3810600
hg1910600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14094018
Samplessample7
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115712
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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