A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554411



Internal ID16341820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:50456822..50807137hg38UCSC Ensembl
Innerchr11:50415993..50766308hg19UCSC Ensembl
Innerchr11:50372569..50722884hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38350316
hg19350316
hg18350316
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1817n54
Supporting Variantsnssv773988
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554411
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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