A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12527



Internal ID9609811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24009191..24605708hg38UCSC Ensembl
Innerchr15:24254338..24850855hg19UCSC Ensembl
Innerchr15:21805431..22401948hg18UCSC Ensembl
Innerchr15:21805431..22401948hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38596518
hg19596518
hg18596518
hg17596518
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758371
Supporting Variants
SamplesNA19207
Known GenesPWRN1, PWRN2
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)essv12527
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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