A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758224



Internal ID9980301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57784622..58059733hg38UCSC Ensembl
Innerchr10:59544382..59819493hg19UCSC Ensembl
Innerchr10:59214388..59489499hg18UCSC Ensembl
Innerchr10:59214388..59489499hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38275112
hg19275112
hg18275112
hg17275112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759760
Supporting Variantsessv6403
SamplesNA18572
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)esv2758224
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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