A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555475



Internal ID16342884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:80417665..80465176hg38UCSC Ensembl
Innerchr11:80128709..80176220hg19UCSC Ensembl
Innerchr11:79806357..79853868hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3847512
hg1947512
hg1847512
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174837
Samples1782681278_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555475
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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