A curated catalogue of human genomic structural variation




Variant Details

Variant: esv995580



Internal ID6731530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54053790..54056986hg38UCSC Ensembl
Innerchr19:54557044..54560240hg19UCSC Ensembl
Innerchr19:59248856..59252052hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg383197
hg193197
hg183197
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586957
SamplesHuRef
Known GenesVSTM1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv995580
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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