A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2757938



Internal ID9980015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:60929127..61102438hg38UCSC Ensembl
Innerchr4:61794845..61968156hg19UCSC Ensembl
Innerchr4:61477440..61650751hg18UCSC Ensembl
Innerchr4:61623611..61796922hg17UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38173312
hg19173312
hg18173312
hg17173312
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759255
Supporting Variantsessv5902, essv3375, essv8593, essv3709, essv24308, essv5512, essv70
SamplesNA18947, NA18550, NA19239, NA18991, NA10856, NA18945, NA18632
Known Genes
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)esv2757938
Frequency
Sample Size270
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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