A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095152



Internal ID21285286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:99477037..99485076hg38UCSC Ensembl
Innerchr14:99943374..99951413hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg388040
hg198040
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115049
Supporting Variants
Samplessample372
Known GenesCCNK, SETD3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095152
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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