A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115728



Internal ID21298994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15133656..15134748hg38UCSC Ensembl
Innerchr4:15135280..15136372hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg381093
hg191093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14107357
Samplessample44
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115728
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