A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154452



Internal ID22084957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13809736..13829548hg38UCSC Ensembl
Outerchr9:13804581..13830117hg38UCSC Ensembl
Innerchr9:13809735..13829547hg19UCSC Ensembl
Outerchr9:13804580..13830116hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3825537
hg1925537
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4006287
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154452
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