A curated catalogue of human genomic structural variation




Variant Details

Variant: essv17907



Internal ID9615788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64061556..64334167hg38UCSC Ensembl
Innerchr20:62692909..62965520hg19UCSC Ensembl
Innerchr20:62163353..62435964hg18UCSC Ensembl
Innerchr20:62163353..62435964hg17UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38272612
hg19272612
hg18272612
hg17272612
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758527
Supporting Variants
SamplesNA12003
Known GenesC20orf201, LINC00266-1, MIR6813, MYT1, NPBWR2, OPRL1, PCMTD2, RGS19, TCEA2
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)essv17907
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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