A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586133



Internal ID6710829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:52547145..52551659hg38UCSC Ensembl
Innerchr15:52839342..52843856hg19UCSC Ensembl
Innerchr15:50626634..50631148hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg384515
hg194515
hg184515
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1001541
Supporting Variants
SamplesHuRef
Known GenesARPP19
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586133
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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