A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553550



Internal ID15994273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:13276938..13277953hg38UCSC Ensembl
Innerchr11:13298485..13299500hg19UCSC Ensembl
Innerchr11:13255061..13256076hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg381016
hg191016
hg181016
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1658n54
Supporting Variantsnssv768257
Samples
Known GenesARNTL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553550
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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