A curated catalogue of human genomic structural variation




Variant Details

Variant: essv19919



Internal ID9618023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31646275..32165340hg38UCSC Ensembl
Innerchr15:31938478..32457541hg19UCSC Ensembl
Innerchr15:29725770..30244833hg18UCSC Ensembl
Innerchr15:29725770..30244833hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38519066
hg19519064
hg18519064
hg17519064
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758375
Supporting Variants
SamplesNA12813
Known GenesCHRNA7, OTUD7A
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)essv19919
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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