A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7266



Internal ID9629158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:1363005..1546611hg38UCSC Ensembl
Innerchr3:1404689..1588295hg19UCSC Ensembl
Innerchr3:1379689..1563295hg18UCSC Ensembl
Innerchr3:1379689..1563295hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38183607
hg19183607
hg18183607
hg17183607
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2757854, esv2757855
Supporting Variants
SamplesNA18592
Known GenesCNTN6
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)essv7266
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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