A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2757811



Internal ID9979888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:77899263..78483906hg38UCSC Ensembl
Innerchr2:78126389..78711032hg19UCSC Ensembl
Innerchr2:77979897..78564540hg18UCSC Ensembl
Innerchr2:78038044..78622687hg17UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38584644
hg19584644
hg18584644
hg17584644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759068
Supporting Variantsessv12983, essv7794
SamplesNA18558, NA18859
Known GenesSNAR-H
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)esv2757811
Frequency
Sample Size270
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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