A curated catalogue of human genomic structural variation




Variant Details

Variant: essv24224



Internal ID9622808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31646275..32240934hg38UCSC Ensembl
Innerchr15:31938478..32533135hg19UCSC Ensembl
Innerchr15:29725770..30320427hg18UCSC Ensembl
Innerchr15:29725770..30320427hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38594660
hg19594658
hg18594658
hg17594658
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758375
Supporting Variants
SamplesNA10856
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)essv24224
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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