A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100711



Internal ID21282761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:17957518..17959735hg38UCSC Ensembl
Innerchr20:17938162..17940378hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg382218
hg192217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113045
Supporting Variants
Samplessample331
Known GenesSNX5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100711
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