A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117413



Internal ID21300679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:74060125..74064404hg38UCSC Ensembl
Innerchr5:73355950..73360229hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg384280
hg194280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097500
Samplessample135
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117413
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