A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16338



Internal ID9614045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:167813440..168130542hg38UCSC Ensembl
Innerchr4:168734591..169051693hg19UCSC Ensembl
Innerchr4:168971166..169288268hg18UCSC Ensembl
Innerchr4:169109321..169426423hg17UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38317103
hg19317103
hg18317103
hg17317103
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2757967
Supporting Variants
SamplesNA19193
Known GenesANXA10
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)essv16338
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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