A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095118



Internal ID21284407
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 StatusS
Merged Variantsnsv3111434
Supporting Variants
Samplessample360
Known GenesSPTLC2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095118
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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