A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111246



Internal ID21294512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:82856003..83491797hg38UCSC Ensembl
Innerchr9:85470918..86106712hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38635795
hg19635795
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089467
Samplessample42
Known GenesFRMD3, RASEF
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111246
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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