A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053427



Internal ID18795958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1301363..1387501hg38UCSC Ensembl
Innerchr11:1322593..1408731hg19UCSC Ensembl
Innerchr11:1279169..1365307hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3886139
hg1986139
hg1886139
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3522464
Samples
Known GenesTOLLIP, TOLLIP-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053427
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