A curated catalogue of human genomic structural variation




Variant Details

Variant: essv84195



Internal ID11394142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20344784..20995430hg38UCSC Ensembl
Innerchr15:20550037..21200759hg19UCSC Ensembl
Innerchr15:18810051..19465418hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38650647
hg19650723
hg18655368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv29956
Supporting Variants
SamplesWATSON
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, POTEB, POTEB2
MethodOligo aCGH
AnalysisThe data were analyzed using the CGH Analytics software.
PlatformAgilent-014584 Human Genome 244K CGH Microarray (Alpha Test)
Comments
ReferenceWheeler_et_al_2008
Pubmed ID18421352
Accession Number(s)essv84195
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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