A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113986



Internal ID21297252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:124251317..124299768hg38UCSC Ensembl
Innerchr9:127013596..127062047hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3848452
hg1948452
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088417
Samplessample11
Known GenesNEK6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113986
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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