A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089873



Internal ID21285622
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 StatusS
Merged Variantsnsv3115147
Supporting Variants
Samplessample378
Known GenesINPP5A, NKX6-2, TTC40
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089873
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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