A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083531



Internal ID21279262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:78811346..78814066hg38UCSC Ensembl
Innerchr6:79521063..79523783hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg382721
hg192721
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117934
Supporting Variants
Samplessample28
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083531
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