A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089913



Internal ID21287669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12461317..12491527hg38UCSC Ensembl
Innerchr10:12503316..12533526hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3830211
hg1930211
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115145
Supporting Variants
Samplessample404
Known GenesCAMK1D
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089913
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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