A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092082



Internal ID21274416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:48710262..48719710hg38UCSC Ensembl
Innerchr4:48712279..48721727hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg389449
hg199449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110298
Supporting Variants
Samplessample207
Known GenesFRYL
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092082
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