A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758058



Internal ID9633517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:62996717..63275984hg38UCSC Ensembl
Innerchr6:63706622..63985889hg19UCSC Ensembl
Innerchr6:63764581..64043848hg18UCSC Ensembl
Innerchr6:63764581..64043848hg17UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38279268
hg19279268
hg18279268
hg17279268
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759434
Supporting Variantsessv3519
SamplesNA18965
Known GenesLGSN
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)esv2758058
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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