A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554030



Internal ID16341439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38224335..38304833hg38UCSC Ensembl
Innerchr11:38245885..38326383hg19UCSC Ensembl
Innerchr11:38202461..38282959hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3880499
hg1980499
hg1880499
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1749n54
Supporting Variantsnssv771087
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554030
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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