A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115141



Internal ID21298407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:96530862..96701803hg38UCSC Ensembl
Innerchr9:99293144..99464085hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38170942
hg19170942
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088833
Samplessample395
Known GenesAAED1, CDC14B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115141
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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