A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11n50



Internal ID22767840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5755980..5788247hg38UCSC Ensembl
chr11:5777210..5809477hg19UCSC Ensembl
chr11:5733786..5766053hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3832268
hg1932268
hg1832268
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv512205, nsv511480
Samples1
Known GenesOR52N1, OR52N5
MethodSequencing
SNP array
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
Analysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Not reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)dgv11n50
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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