A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758071



Internal ID9980148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:102700861..102858064hg38UCSC Ensembl
Innerchr6:103148736..103305939hg19UCSC Ensembl
Innerchr6:103255429..103412632hg18UCSC Ensembl
Innerchr6:103255429..103412632hg17UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38157204
hg19157204
hg18157204
hg17157204
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759459
Supporting Variantsessv1914
SamplesNA18959
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)esv2758071
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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