A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118055



Internal ID21301321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:24081843..24086979hg38UCSC Ensembl
Innerchr4:24083466..24088602hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg385137
hg195137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14092151
Samplessample221
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118055
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