A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093224



Internal ID21284394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:102449714..102453865hg38UCSC Ensembl
Innerchr11:102320445..102324596hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg384152
hg194152
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113221
Supporting Variants
Samplessample360
Known GenesTMEM123
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093224
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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