A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758211



Internal ID9980288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19425708..19736065hg38UCSC Ensembl
Innerchr10:19714637..20024994hg19UCSC Ensembl
Innerchr10:19754643..20065000hg18UCSC Ensembl
Innerchr10:19754643..20065000hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38310358
hg19310358
hg18310358
hg17310358
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759737
Supporting Variantsessv7262
SamplesNA18592
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)esv2758211
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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