A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115577



Internal ID21298843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:45093655..45133676hg38UCSC Ensembl
Innerchr6:45061392..45101413hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3840022
hg1940022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14082838
Samplessample9
Known GenesSUPT3H
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115577
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