A curated catalogue of human genomic structural variation




Variant Details

Variant: esv992368



Internal ID7062094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29577282..29580443hg38UCSC Ensembl
Innerchr19:30068189..30071350hg19UCSC Ensembl
Innerchr19:34760029..34763190hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg383162
hg193162
hg183162
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586365
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv992368
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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