A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586017



Internal ID7057399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20351177..20968557hg38UCSC Ensembl
Innerchr15:20556430..21173886hg19UCSC Ensembl
Innerchr15:18816444..19438545hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38617381
hg19617457
hg18622102
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv988919
Supporting Variants
SamplesHuRef
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, POTEB, POTEB2
MethodSNP array
AnalysisPooled samples.
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586017
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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