A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2757930



Internal ID9980007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:32398708..32569327hg38UCSC Ensembl
Innerchr4:32400330..32570949hg19UCSC Ensembl
Innerchr4:32044228..32214847hg18UCSC Ensembl
Innerchr4:32190399..32361018hg17UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38170620
hg19170620
hg18170620
hg17170620
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759245
Supporting Variantsessv10698
SamplesNA18855
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)esv2757930
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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