A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093046



Internal ID21279694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:16873175..16893715hg38UCSC Ensembl
Innerchr11:16894722..16915262hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3820541
hg1920541
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112278
Supporting Variants
Samplessample287
Known GenesPLEKHA7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093046
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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