A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116908



Internal ID21300174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73783661..73788770hg38UCSC Ensembl
Innerchr14:74250364..74255473hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg385110
hg195110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14095532
Samplessample208
Known GenesELMSAN1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116908
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