A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154776



Internal ID22085281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:112268501..112272273hg38UCSC Ensembl
Outerchr11:112266674..112277057hg38UCSC Ensembl
Innerchr11:112139224..112142996hg19UCSC Ensembl
Outerchr11:112137397..112147780hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3810384
hg1910384
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4007316
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154776
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