A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758243



Internal ID9980320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:123297701..123509643hg38UCSC Ensembl
Innerchr10:125057217..125269159hg19UCSC Ensembl
Innerchr10:125047207..125259149hg18UCSC Ensembl
Innerchr10:125047207..125259149hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38211943
hg19211943
hg18211943
hg17211943
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759787
Supporting Variantsessv6317, essv7108, essv23082, essv3282, essv6405, essv16646
SamplesNA12812, NA18572, NA18537, NA19142, NA18609, NA18972
Known Genes
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)esv2758243
Frequency
Sample Size270
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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