A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115734



Internal ID21299000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:135969084..135997842hg38UCSC Ensembl
Innerchr5:135304773..135333531hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3828759
hg1928759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14109147, nssv14082699, nssv14108460
Samplessample402, sample153, sample253
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115734
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer