A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2757856



Internal ID9633315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2164588..2453733hg38UCSC Ensembl
Innerchr3:2206272..2495417hg19UCSC Ensembl
Innerchr3:2181272..2470417hg18UCSC Ensembl
Innerchr3:2181272..2470417hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38289146
hg19289146
hg18289146
hg17289146
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759124
Supporting Variantsessv7276
SamplesNA18592
Known GenesCNTN4
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)esv2757856
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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