A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054339



Internal ID18796870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8132035..8241626hg38UCSC Ensembl
Innerchr11:8153582..8263173hg19UCSC Ensembl
Innerchr11:8110158..8219749hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38109592
hg19109592
hg18109592
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3708513
Samples
Known GenesLMO1, RIC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054339
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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