A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759297



Internal ID9981442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:161813465..161986813hg38UCSC Ensembl
Innerchr4:162734617..162907965hg19UCSC Ensembl
Innerchr4:162954067..163127415hg18UCSC Ensembl
Innerchr4:163092222..163265570hg17UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg38173349
hg19173349
hg18173349
hg17173349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2757964
SamplesNA19193
Known GenesFSTL5
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)esv2759297
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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