A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554099



Internal ID16341508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:41784151..41797265hg38UCSC Ensembl
Innerchr11:41805701..41818815hg19UCSC Ensembl
Innerchr11:41762277..41775391hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3813115
hg1913115
hg1813115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1759n54
Supporting Variantsnssv771181, nssv771182
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554099
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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