A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759277



Internal ID9981422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:115343092..115530641hg38UCSC Ensembl
Innerchr4:116264248..116451797hg19UCSC Ensembl
Innerchr4:116483697..116671246hg18UCSC Ensembl
Innerchr4:116621852..116809401hg17UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38187550
hg19187550
hg18187550
hg17187550
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2757950
SamplesNA19193
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)esv2759277
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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