A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089306



Internal ID21267373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:56906772..56909706hg38UCSC Ensembl
Innerchr4:57772938..57775872hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg382935
hg192935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115259
Supporting Variants
Samplessample111
Known GenesREST
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089306
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