A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9801



Internal ID9631975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:117110061..117283106hg38UCSC Ensembl
Innerchr6:117431224..117604269hg19UCSC Ensembl
Innerchr6:117537917..117710962hg18UCSC Ensembl
Innerchr6:117537917..117710962hg17UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38173046
hg19173046
hg18173046
hg17173046
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758076
Supporting Variants
SamplesNA18863
Known GenesVGLL2
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)essv9801
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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