A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2757868



Internal ID9633327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41297661..41732261hg38UCSC Ensembl
Innerchr3:41339152..41773753hg19UCSC Ensembl
Innerchr3:41314156..41748757hg18UCSC Ensembl
Innerchr3:41314156..41748757hg17UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38434601
hg19434602
hg18434602
hg17434602
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759143
Supporting Variantsessv3708
SamplesNA18947
Known GenesULK4
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)esv2757868
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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