A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554819



Internal ID15995542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55600413..55627975hg38UCSC Ensembl
Innerchr11:55367889..55395451hg19UCSC Ensembl
Innerchr11:55124465..55152027hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3827563
hg1927563
hg1827563
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv775198
Samples
Known GenesOR4C11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554819
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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