A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117195



Internal ID21300461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133065120..133090666hg38UCSC Ensembl
Innerchr9:135940507..135966053hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3825547
hg1925547
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089542, nssv14088010
Samplessample71, sample290
Known GenesCEL, CELP
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117195
Frequency
Sample Size467
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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