A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759310



Internal ID9981455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186340176..186501188hg38UCSC Ensembl
Innerchr4:187261330..187422342hg19UCSC Ensembl
Innerchr4:187498324..187659336hg18UCSC Ensembl
Innerchr4:187636479..187797491hg17UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38161013
hg19161013
hg18161013
hg17161013
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2757972
SamplesNA18999, NA12812, NA18547, NA18532, NA18608, NA18953, NA18609, NA07000
Known GenesF11-AS1
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)esv2759310
Frequency
Sample Size270
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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