A curated catalogue of human genomic structural variation




Variant Details

Variant: essv902



Internal ID9631107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:25721356..26086930hg38UCSC Ensembl
Innerchr20:25701992..26067566hg19UCSC Ensembl
Innerchr20:25649992..26015566hg18UCSC Ensembl
Innerchr20:25649992..26015566hg17UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38365575
hg19365575
hg18365575
hg17365575
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758517
Supporting Variants
SamplesNA19000
Known GenesFAM182A, FAM182B, LOC100134868
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)essv902
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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