A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759242



Internal ID9981387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:29522020..29689455hg38UCSC Ensembl
Innerchr4:29523642..29691077hg19UCSC Ensembl
Innerchr4:29132740..29300175hg18UCSC Ensembl
Innerchr4:29199911..29367346hg17UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38167436
hg19167436
hg18167436
hg17167436
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2757927
SamplesNA19003
Known Genes
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)esv2759242
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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