A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101369



Internal ID21281130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40855307..40878645hg38UCSC Ensembl
Innerchr19:41361212..41384550hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3823339
hg1923339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113598
Supporting Variants
Samplessample308
Known GenesCYP2A7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101369
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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