A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586957



Internal ID6711653
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv995580
Supporting Variants
SamplesHuRef
Known GenesVSTM1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586957
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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