A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554418



Internal ID16341827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:50516440..50800919hg38UCSC Ensembl
Innerchr11:50475611..50760090hg19UCSC Ensembl
Innerchr11:50432187..50716666hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38284480
hg19284480
hg18284480
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1820n54
Supporting Variantsnssv774008
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554418
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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