A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116278



Internal ID21299544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:73258177..73349731hg38UCSC Ensembl
Innerchr9:75873093..75964647hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3891555
hg1991555
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089535
Samplessample70
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116278
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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