A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113119



Internal ID21296385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:17540842..17567072hg38UCSC Ensembl
Innerchr4:17542465..17568695hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3826231
hg1926231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv861n145
Supporting Variantsnssv14092226
Samplessample235
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113119
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