A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758096



Internal ID9633555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:169346196..169434098hg38UCSC Ensembl
Innerchr6:169746291..169834193hg19UCSC Ensembl
Innerchr6:169488216..169576118hg18UCSC Ensembl
Innerchr6:169563923..169651825hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3887903
hg1987903
hg1887903
hg1787903
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759496
Supporting Variantsessv9069, essv23812
SamplesNA19132, NA12763
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)esv2758096
Frequency
Sample Size270
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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