A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15892



Internal ID9613549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31901556..32105050hg38UCSC Ensembl
Innerchr15:32193759..32397251hg19UCSC Ensembl
Innerchr15:29981051..30184543hg18UCSC Ensembl
Innerchr15:29981051..30184543hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38203495
hg19203493
hg18203493
hg17203493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758375
Supporting Variants
SamplesNA19223
Known GenesCHRNA7
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)essv15892
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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