A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088905



Internal ID21280581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:17561468..17611369hg38UCSC Ensembl
Innerchr10:17603467..17653368hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg3849902
hg1949902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115371
Supporting Variants
Samplessample3
Known GenesPTPLA
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088905
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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