A curated catalogue of human genomic structural variation




Variant Details

Variant: essv22238



Internal ID9620601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24009191..24357555hg38UCSC Ensembl
Innerchr15:24254338..24602702hg19UCSC Ensembl
Innerchr15:21805431..22153795hg18UCSC Ensembl
Innerchr15:21805431..22153795hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38348365
hg19348365
hg18348365
hg17348365
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758371
Supporting Variants
SamplesNA12044
Known GenesPWRN2
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)essv22238
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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