A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11267



Internal ID9977437
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 StatusS
Merged Variantsesv2758433
Supporting Variants
SamplesNA19204
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)essv11267
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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