A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083746



Internal ID21291373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:18259972..18265534hg38UCSC Ensembl
Innerchr6:18260203..18265765hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg385563
hg195563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114397
Supporting Variants
Samplessample72
Known GenesDEK
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083746
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