A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758087



Internal ID9980164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:153816648..153973314hg38UCSC Ensembl
Innerchr6:154137783..154294449hg19UCSC Ensembl
Innerchr6:154179476..154336142hg18UCSC Ensembl
Innerchr6:154229897..154386563hg17UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38156667
hg19156667
hg18156667
hg17156667
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759479
Supporting Variantsessv7264, essv24854, essv5088, essv4504, essv73, essv5919, essv3465, essv524
SamplesNA18998, NA18592, NA18550, NA18991, NA18992, NA18552, NA07000, NA18577
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)esv2758087
Frequency
Sample Size270
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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