A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758206



Internal ID9633665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:137991111..138262981hg38UCSC Ensembl
Innerchr9:140885563..141153431hg19UCSC Ensembl
Innerchr9:140005384..140273252hg18UCSC Ensembl
Innerchr9:138161400..138429268hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38271871
hg19267869
hg18267869
hg17267869
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759722
Supporting Variantsessv8136, essv18584, essv15430, essv15998, essv4744, essv22941, essv9092, essv10690, essv11112, essv12643, essv14687, essv23949, essv11714, essv8870, essv10927, essv24231, essv9646, essv11289, essv9377, essv13801, essv8281, essv10351, essv16688, essv12252, essv15792, essv14281, essv16878
SamplesNA19141, NA19203, NA19204, NA18508, NA12814, NA18855, NA07357, NA19131, NA19159, NA19209, NA19194, NA19205, NA19103, NA12234, NA19142, NA19154, NA18853, NA19101, NA19132, NA10856, NA19206, NA18501, NA19211, NA18500, NA18506, NA19153, NA18620
Known GenesCACNA1B, FAM157B, TUBBP5
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)esv2758206
Frequency
Sample Size270
Observed Gain27
Observed Loss0
Observed Complex0
Frequencyn/a


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