A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553446



Internal ID16340855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8247858..8256650hg38UCSC Ensembl
Innerchr11:8269405..8278197hg19UCSC Ensembl
Innerchr11:8225981..8234773hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg388793
hg198793
hg188793
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv767049
Samples
Known GenesLMO1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553446
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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