A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553282



Internal ID16340691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5738876..5740268hg38UCSC Ensembl
Innerchr11:5760106..5761498hg19UCSC Ensembl
Innerchr11:5716682..5718074hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381393
hg191393
hg181393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1610n54
Supporting Variantsnssv765581, nssv765582
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553282
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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