A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511466



Internal ID15850891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:65874656..65874872hg38UCSC Ensembl
Outerchr11:65873435..65874970hg38UCSC Ensembl
Innerchr11:65642127..65642343hg19UCSC Ensembl
Outerchr11:65640906..65642441hg19UCSC Ensembl
Innerchr11:65398703..65398919hg18UCSC Ensembl
Outerchr11:65397482..65399017hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381536
hg191536
hg181536
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626081
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)nsv511466
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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