A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518919



Internal ID15099526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:66641938..66700998hg38UCSC Ensembl
Innerchr11:66409409..66468469hg19UCSC Ensembl
Innerchr11:66165985..66225045hg18UCSC Ensembl
Innerchr11:66165985..66225045hg17UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3859061
hg1959061
hg1859061
hg1759061
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696380
Samples
Known GenesRBM14-RBM4, RBM4, RBM4B, SPTBN2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518919
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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