A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758433



Internal ID9980510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78220032..78337741hg38UCSC Ensembl
Innerchr16:78253929..78371638hg19UCSC Ensembl
Innerchr16:76811430..76929139hg18UCSC Ensembl
Innerchr16:76811430..76929139hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38117710
hg19117710
hg18117710
hg17117710
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2758660
Supporting Variantsessv11267, essv16844
SamplesNA19204, NA19205
Known GenesWWOX
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)esv2758433
Frequency
Sample Size270
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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