A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111393



Internal ID21294659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:127762845..127796162hg38UCSC Ensembl
Innerchr11:127632740..127666057hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3833318
hg1933318
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv230n145
Supporting Variantsnssv14092003
Samplessample270
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111393
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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