A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9458



Internal ID9631593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:79062895..79226427hg38UCSC Ensembl
Innerchr15:79355237..79518769hg19UCSC Ensembl
Innerchr15:77142292..77305824hg18UCSC Ensembl
Innerchr15:77142292..77305824hg17UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38163533
hg19163533
hg18163533
hg17163533
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758389
Supporting Variants
SamplesNA19208
Known GenesLOC729911, MIR184, RASGRF1
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)essv9458
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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