A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758230



Internal ID9980307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:75676822..76010691hg38UCSC Ensembl
Innerchr10:77436580..77770449hg19UCSC Ensembl
Innerchr10:77106586..77440455hg18UCSC Ensembl
Innerchr10:77106586..77440455hg17UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38333870
hg19333870
hg18333870
hg17333870
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759768
Supporting Variantsessv20385, essv7845, essv23601, essv17709, essv12623
SamplesNA18558, NA12872, NA10830, NA18500, NA12006
Known GenesC10orf11
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)esv2758230
Frequency
Sample Size270
Observed Gain1
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer