A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5102



Internal ID9626755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32111710..32332547hg38UCSC Ensembl
Innerchr15:32403911..32624748hg19UCSC Ensembl
Innerchr15:30191203..30412040hg18UCSC Ensembl
Innerchr15:30191203..30412040hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38220838
hg19220838
hg18220838
hg17220838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758375
Supporting Variants
SamplesNA18577
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)essv5102
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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