A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2757961



Internal ID9980038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:157230735..157461136hg38UCSC Ensembl
Innerchr4:158151887..158382288hg19UCSC Ensembl
Innerchr4:158371337..158601738hg18UCSC Ensembl
Innerchr4:158509492..158739893hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38230402
hg19230402
hg18230402
hg17230402
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759291
Supporting Variantsessv9655
SamplesNA18913
Known GenesGRIA2
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)esv2757961
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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