A curated catalogue of human genomic structural variation




Variant Details

Variant: essv17442



Internal ID9957750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:81649179..81931728hg38UCSC Ensembl
Innerchr15:81941520..82224069hg19UCSC Ensembl
Innerchr15:79728575..80011124hg18UCSC Ensembl
Innerchr15:79728575..80011124hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38282550
hg19282550
hg18282550
hg17282550
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758390
Supporting Variants
SamplesNA12043
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)essv17442
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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