A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758093



Internal ID9980170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:165728153..165885447hg38UCSC Ensembl
Innerchr6:166141641..166298935hg19UCSC Ensembl
Innerchr6:166061631..166218925hg18UCSC Ensembl
Innerchr6:166112052..166269346hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38157295
hg19157295
hg18157295
hg17157295
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759491
Supporting Variantsessv23686
SamplesNA10863
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)esv2758093
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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