A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758209



Internal ID9633668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5595145..5762817hg38UCSC Ensembl
Innerchr10:5637108..5804780hg19UCSC Ensembl
Innerchr10:5677111..5844786hg18UCSC Ensembl
Innerchr10:5677111..5844786hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38167673
hg19167673
hg18167676
hg17167676
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759729
Supporting Variantsessv14514, essv9028
SamplesNA19202, NA19132
Known GenesASB13, FAM208B
MethodBAC aCGH
AnalysisArray images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd).
PlatformAgilent
Comments
ReferenceRedon_et_al_2006
Pubmed ID17122850
Accession Number(s)esv2758209
Frequency
Sample Size270
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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