A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094447



Internal ID21291646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:37174639..37187989hg38UCSC Ensembl
Innerchr13:37748776..37762126hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3813351
hg1913351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112114
Supporting Variants
Samplessample77
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094447
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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