A curated catalogue of human genomic structural variation




Variant Details

Variant: essv19188



Internal ID9617211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32559051..32574849hg38UCSC Ensembl
Innerchr6:32526828..32542626hg19UCSC Ensembl
Innerchr6:32634806..32650604hg18UCSC Ensembl
Innerchr6:32634806..32650604hg17UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3815799
hg1915799
hg1815799
hg1715799
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758044
Supporting Variants
SamplesNA12865
Known GenesHLA-DRB6
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)essv19188
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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