A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12270



Internal ID9609526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14061..178465hg38UCSC Ensembl
Innerchr10:60001..224405hg19UCSC Ensembl
Innerchr10:50001..214405hg18UCSC Ensembl
Innerchr10:50001..214405hg17UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38164405
hg19164405
hg18164405
hg17164405
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758207
Supporting Variants
SamplesNA19101
Known GenesTUBB8, ZMYND11
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)essv12270
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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