A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100141



Internal ID21279143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:79638880..79713578hg38UCSC Ensembl
Innerchr18:77398880..77473578hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3874699
hg1974699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112200
Supporting Variants
Samplessample278
Known GenesCTDP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100141
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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