A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14095



Internal ID9611553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:117110061..117306112hg38UCSC Ensembl
Innerchr6:117431224..117627275hg19UCSC Ensembl
Innerchr6:117537917..117733968hg18UCSC Ensembl
Innerchr6:117537917..117733968hg17UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38196052
hg19196052
hg18196052
hg17196052
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758076
Supporting Variants
SamplesNA18861
Known GenesROS1, VGLL2
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)essv14095
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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