A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511476



Internal ID15850901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:46139524..46140691hg38UCSC Ensembl
Outerchr11:46139503..46148108hg38UCSC Ensembl
Innerchr11:46161075..46162242hg19UCSC Ensembl
Outerchr11:46161054..46169659hg19UCSC Ensembl
Innerchr11:46117651..46118818hg18UCSC Ensembl
Outerchr11:46117630..46126235hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg388606
hg198606
hg188606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626092
Samples1
Known Genes
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511476
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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