A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552888



Internal ID16340297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:841959..846738hg38UCSC Ensembl
Innerchr11:841959..846738hg19UCSC Ensembl
Innerchr11:831959..836738hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg384780
hg194780
hg184780
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv763586
Samples
Known GenesPOLR2L, TSPAN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552888
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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