A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759477



Internal ID9981622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:150967072..151133703hg38UCSC Ensembl
Innerchr6:151288208..151454839hg19UCSC Ensembl
Innerchr6:151329901..151496532hg18UCSC Ensembl
Innerchr6:151380322..151546953hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38166632
hg19166632
hg18166632
hg17166632
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758085
SamplesNA18563
Known GenesMTHFD1L
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)esv2759477
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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