A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154668



Internal ID22085173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:274325..372369hg38UCSC Ensembl
Outerchr11:270715..377795hg38UCSC Ensembl
Innerchr11:274325..372369hg19UCSC Ensembl
Outerchr11:270715..377795hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38107081
hg19107081
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4005524
Samples
Known GenesATHL1, B4GALNT4, IFITM1, IFITM2, IFITM3, IFITM5, NLRP6
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154668
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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