A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111434



Internal ID21294700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:77613454..77620077hg38UCSC Ensembl
Innerchr14:78079797..78086420hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg386624
hg196624
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14095118
Samplessample360
Known GenesSPTLC2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111434
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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