A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094433



Internal ID21290986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:29371809..29390700hg38UCSC Ensembl
Innerchr13:29945946..29964837hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3818892
hg1918892
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117040
Supporting Variants
Samplessample68
Known GenesMTUS2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094433
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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