A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2757926



Internal ID9980003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:28542336..28837815hg38UCSC Ensembl
Innerchr4:28543958..28839437hg19UCSC Ensembl
Innerchr4:28153056..28448535hg18UCSC Ensembl
Innerchr4:28220227..28515706hg17UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38295480
hg19295480
hg18295480
hg17295480
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759239
Supporting Variantsessv1942
SamplesNA18959
Known GenesMIR4275
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)esv2757926
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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