A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758819



Internal ID9634278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:31857279..32144529hg38UCSC Ensembl
Innerchr21:33229592..33516840hg19UCSC Ensembl
Innerchr21:32151463..32438711hg18UCSC Ensembl
Innerchr21:32151463..32438711hg17UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38287251
hg19287249
hg18287249
hg17287249
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758533
SamplesNA19205, NA19173
Known GenesHUNK, LINC00159
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)esv2758819
Frequency
Sample Size270
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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