A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759473



Internal ID9634932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:137138391..137252201hg38UCSC Ensembl
Innerchr6:137459528..137573338hg19UCSC Ensembl
Innerchr6:137501221..137615031hg18UCSC Ensembl
Innerchr6:137501221..137615031hg17UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38113811
hg19113811
hg18113811
hg17113811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758082
SamplesNA18991
Known GenesIFNGR1, IL22RA2
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)esv2759473
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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