A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4177



Internal ID9625726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24335344..24499496hg38UCSC Ensembl
Innerchr15:24580491..24744643hg19UCSC Ensembl
Innerchr15:22131584..22295736hg18UCSC Ensembl
Innerchr15:22131584..22295736hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38164153
hg19164153
hg18164153
hg17164153
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758371
Supporting Variants
SamplesNA18555
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)essv4177
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer