A curated catalogue of human genomic structural variation




Variant Details

Variant: esv987659



Internal ID6723633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54052552..54057223hg38UCSC Ensembl
Innerchr19:54555806..54560477hg19UCSC Ensembl
Innerchr19:59247618..59252289hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg384672
hg194672
hg184672
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586739
SamplesHuRef
Known GenesVSTM1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv987659
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer