A curated catalogue of human genomic structural variation




Variant Details

Variant: essv21211



Internal ID9619461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31646275..32295702hg38UCSC Ensembl
Innerchr15:31938478..32587903hg19UCSC Ensembl
Innerchr15:29725770..30375195hg18UCSC Ensembl
Innerchr15:29725770..30375195hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38649428
hg19649426
hg18649426
hg17649426
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758375
Supporting Variants
SamplesNA11830
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)essv21211
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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