A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759029



Internal ID9981174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:15062065..15217735hg38UCSC Ensembl
Innerchr2:15202189..15357859hg19UCSC Ensembl
Innerchr2:15119640..15275310hg18UCSC Ensembl
Innerchr2:15152787..15308457hg17UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38155671
hg19155671
hg18155671
hg17155671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2757786
SamplesNA18852
Known GenesNBAS
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)esv2759029
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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