A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758239



Internal ID9980316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105769904..105993781hg38UCSC Ensembl
Innerchr10:107529662..107753539hg19UCSC Ensembl
Innerchr10:107519652..107743529hg18UCSC Ensembl
Innerchr10:107519652..107743529hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38223878
hg19223878
hg18223878
hg17223878
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759780
Supporting Variantsessv21421, essv16473, essv16221, essv19512, essv18930, essv6961, essv4665, essv5152, essv24223, essv5305, essv23624, essv13145, essv24699, essv5459, essv3022, essv10357, essv10114, essv7119, essv443, essv17798, essv14698, essv19913, essv18361, essv10590, essv17295, essv21028, essv135, essv21135, essv4920, essv17937, essv23212
SamplesNA12717, NA11829, NA18561, NA12813, NA18563, NA18582, NA19130, NA12005, NA12156, NA11994, NA12815, NA19159, NA12003, NA10831, NA19161, NA18981, NA18537, NA18856, NA10856, NA18632, NA06991, NA18952, NA12864, NA18564, NA19240, NA18594, NA18506, NA19102, NA18968, NA19139, NA12006
Known Genes
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)esv2758239
Frequency
Sample Size270
Observed Gain14
Observed Loss17
Observed Complex0
Frequencyn/a


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