A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10114



Internal ID9974397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105839536..105993781hg38UCSC Ensembl
Innerchr10:107599294..107753539hg19UCSC Ensembl
Innerchr10:107589284..107743529hg18UCSC Ensembl
Innerchr10:107589284..107743529hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38154246
hg19154246
hg18154246
hg17154246
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758239
Supporting Variants
SamplesNA19130
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)essv10114
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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