A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554073



Internal ID16341482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38950400..39051419hg38UCSC Ensembl
Innerchr11:38971950..39072969hg19UCSC Ensembl
Innerchr11:38928526..39029545hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38101020
hg19101020
hg18101020
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174638
SamplesHGDP00822
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554073
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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