A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16899



Internal ID9614667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24335344..24655767hg38UCSC Ensembl
Innerchr15:24580491..24900914hg19UCSC Ensembl
Innerchr15:22131584..22452007hg18UCSC Ensembl
Innerchr15:22131584..22452007hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38320424
hg19320424
hg18320424
hg17320424
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758371
Supporting Variants
SamplesNA19205
Known GenesPWRN1
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)essv16899
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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