A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093003



Internal ID21288989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:31007179..31009219hg38UCSC Ensembl
Innerchr13:31581316..31583356hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg382041
hg192041
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114172
Supporting Variants
Samplessample424
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093003
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