A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090876



Internal ID21292007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:108496543..108501638hg38UCSC Ensembl
Innerchr11:108367270..108372365hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg385096
hg195096
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111737
Supporting Variants
Samplessample81
Known GenesKDELC2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090876
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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