A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093024



Internal ID21279102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:35222398..35238346hg38UCSC Ensembl
Innerchr11:35243945..35259893hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3815949
hg1915949
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113810
Supporting Variants
Samplessample278
Known GenesCD44
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093024
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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