A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554822



Internal ID15995545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55600413..55630541hg38UCSC Ensembl
Innerchr11:55367889..55398017hg19UCSC Ensembl
Innerchr11:55124465..55154593hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3830129
hg1930129
hg1830129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1910n54
Supporting Variantsnssv775201
Samples
Known GenesOR4C11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554822
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer