A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4006746



Internal ID22068377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37184385..37205385hg38UCSC Ensembl
Outerchr11:37183857..37213290hg38UCSC Ensembl
Innerchr11:37205935..37226935hg19UCSC Ensembl
Outerchr11:37205407..37234840hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3829434
hg1929434
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154713
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4006746
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