A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005181



Internal ID7070277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40876680..40881358hg38UCSC Ensembl
Innerchr19:41382585..41387263hg19UCSC Ensembl
Innerchr19:46074425..46079103hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg384679
hg194679
hg184679
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587133
SamplesHuRef
Known GenesCYP2A7
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005181
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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