A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758247



Internal ID9980324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132852198..133019862hg38UCSC Ensembl
Innerchr10:134665702..134833366hg19UCSC Ensembl
Innerchr10:134515692..134683356hg18UCSC Ensembl
Innerchr10:134515692..134683302hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38167665
hg19167665
hg18167665
hg17167611
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759792
Supporting Variantsessv22058
SamplesNA12154
Known GenesLOC399829, TTC40
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)esv2758247
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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