A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556486



Internal ID16343895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:123819624..123853238hg38UCSC Ensembl
Innerchr11:123690332..123723946hg19UCSC Ensembl
Innerchr11:123195542..123229156hg18UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3833615
hg1933615
hg1833615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv784648
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556486
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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