A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13155



Internal ID9610509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75566792..75865641hg38UCSC Ensembl
Innerchr3:75615943..75914792hg19UCSC Ensembl
Innerchr3:75698633..75997482hg18UCSC Ensembl
Innerchr3:75698633..75997482hg17UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38298850
hg19298850
hg18298850
hg17298850
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2757874, esv2757875
Supporting Variants
SamplesNA19102
Known GenesFLJ20518, FRG2C, LINC00960, MIR1324, MIR4273, ZNF717
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)essv13155
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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