A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758238



Internal ID9633697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:100619878..100805979hg38UCSC Ensembl
Innerchr10:102379635..102565736hg19UCSC Ensembl
Innerchr10:102369625..102555726hg18UCSC Ensembl
Innerchr10:102369625..102555726hg17UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg38186102
hg19186102
hg18186102
hg17186102
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759779
Supporting Variantsessv14536, essv24916
SamplesNA19202, NA06994
Known GenesPAX2
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)esv2758238
Frequency
Sample Size270
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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