A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758078



Internal ID9980155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:128521047..128523686hg38UCSC Ensembl
Innerchr6:128842192..128844831hg19UCSC Ensembl
Innerchr6:128883885..128886524hg18UCSC Ensembl
Innerchr6:128883885..128886524hg17UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg382640
hg192640
hg182640
hg172640
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759468
Supporting Variantsessv24312
SamplesNA10856
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)esv2758078
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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