A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759199



Internal ID9981344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163884661..164192272hg38UCSC Ensembl
Innerchr3:163602449..163910060hg19UCSC Ensembl
Innerchr3:165085143..165392754hg18UCSC Ensembl
Innerchr3:165085151..165392762hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38307612
hg19307612
hg18307612
hg17307612
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2757903
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)esv2759199
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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