A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106742



Internal ID21284583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:125866877..125910406hg38UCSC Ensembl
Innerchr2:126624454..126667983hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3843530
hg1943530
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114144
Supporting Variants
Samplessample362
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106742
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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