A curated catalogue of human genomic structural variation




Variant Details

Variant: essv23218



Internal ID9621690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32111694..32332547hg38UCSC Ensembl
Innerchr15:32403895..32624748hg19UCSC Ensembl
Innerchr15:30191187..30412040hg18UCSC Ensembl
Innerchr15:30191187..30412040hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38220854
hg19220854
hg18220854
hg17220854
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758375
Supporting Variants
SamplesNA12156
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)essv23218
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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