A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092003



Internal ID21278544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:127762845..127796162hg38UCSC Ensembl
Innerchr11:127632740..127666057hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3833318
hg1933318
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111393
Supporting Variants
Samplessample270
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092003
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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