A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554840



Internal ID15995563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55602150..55624962hg38UCSC Ensembl
Innerchr11:55369626..55392438hg19UCSC Ensembl
Innerchr11:55126202..55149014hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3822813
hg1922813
hg1822813
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1918n54
Supporting Variantsnssv775659, nssv775660
Samples
Known GenesOR4C11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554840
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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