A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759782



Internal ID9981927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:108699229..108883738hg38UCSC Ensembl
Innerchr10:110458987..110643496hg19UCSC Ensembl
Innerchr10:110448977..110633486hg18UCSC Ensembl
Innerchr10:110448977..110633486hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38184510
hg19184510
hg18184510
hg17184510
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758240
SamplesNA10856
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)esv2759782
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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