A curated catalogue of human genomic structural variation




Variant Details

Variant: esv988919



Internal ID7060750
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 Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586017
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)esv988919
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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