A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554839



Internal ID15995562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55602150..55618626hg38UCSC Ensembl
Innerchr11:55369626..55386102hg19UCSC Ensembl
Innerchr11:55126202..55142678hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3816477
hg1916477
hg1816477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1917n54
Supporting Variantsnssv775658, nssv775657
Samples
Known GenesOR4C11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554839
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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