A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101327



Internal ID21280263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:13952338..13957918hg38UCSC Ensembl
Innerchr19:14063150..14068730hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg385581
hg195581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110760
Supporting Variants
Samplessample295
Known GenesDCAF15, PODNL1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101327
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