A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554615



Internal ID16342024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54928232..55259170hg38UCSC Ensembl
Innerchr11:54695707..55026646hg19UCSC Ensembl
Innerchr11:54452283..54783222hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38330939
hg19330940
hg18330940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1864n54
Supporting Variantsnssv774764
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554615
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer