A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759307



Internal ID9981452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:182637163..182821194hg38UCSC Ensembl
Innerchr4:183558316..183742347hg19UCSC Ensembl
Innerchr4:183795310..183979341hg18UCSC Ensembl
Innerchr4:183933465..184117496hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38184032
hg19184032
hg18184032
hg17184032
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2757970
SamplesNA19222
Known GenesTENM3
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)esv2759307
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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