A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096318



Internal ID21278856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:99478539..99484154hg38UCSC Ensembl
Innerchr14:99944876..99950491hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg385616
hg195616
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112528
Supporting Variants
Samplessample275
Known GenesCCNK, SETD3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096318
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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