A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552931



Internal ID15993654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1297082..1387360hg38UCSC Ensembl
Innerchr11:1318312..1408590hg19UCSC Ensembl
Innerchr11:1274888..1365166hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3890279
hg1990279
hg1890279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1537n54
Supporting Variantsnssv763970
Samples
Known GenesTOLLIP, TOLLIP-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552931
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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