A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114144



Internal ID21297410
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 StatusM
Merged Variants
Supporting Variantsnssv14106742
Samplessample362
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114144
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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