A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095865



Internal ID21280231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68072764..68096681hg38UCSC Ensembl
Innerchr13:68646896..68670813hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3823918
hg1923918
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117306
Supporting Variants
Samplessample295
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095865
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