A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115147



Internal ID21298413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132776204..132907359hg38UCSC Ensembl
Innerchr10:134589708..134720863hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38131156
hg19131156
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089873
Samplessample378
Known GenesINPP5A, NKX6-2, TTC40
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115147
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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