A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556482



Internal ID15997205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:122866145..122914109hg38UCSC Ensembl
Innerchr11:122736853..122784817hg19UCSC Ensembl
Innerchr11:122242063..122290027hg18UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3847965
hg1947965
hg1847965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv784644
Samples
Known GenesC11orf63, CRTAM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556482
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