A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113003



Internal ID21296269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:102578214..102639430hg38UCSC Ensembl
Innerchr3:102297058..102358274hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg3861217
hg1961217
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14105405
Samplessample116
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113003
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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