A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116450



Internal ID21299716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38733336..38736637hg38UCSC Ensembl
Innerchr9:38733333..38736634hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg383302
hg193302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088460, nssv14088849
Samplessample402, sample27
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116450
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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