A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094517



Internal ID21267264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:29371809..29388429hg38UCSC Ensembl
Innerchr13:29945946..29962566hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3816621
hg1916621
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113344
Supporting Variants
Samplessample110
Known GenesMTUS2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094517
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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