A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089820



Internal ID21284322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87861038..87866093hg38UCSC Ensembl
Innerchr10:89620795..89625850hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg385056
hg195056
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115954
Supporting Variants
Samplessample360
Known GenesKLLN, PTEN
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089820
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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