A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100344



Internal ID21270486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40835670..40863496hg38UCSC Ensembl
Innerchr19:41341575..41369401hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3827827
hg1927827
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112577
Supporting Variants
Samplessample150
Known GenesCYP2A6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100344
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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