A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14082933



Internal ID21281781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:38165616..38326402hg38UCSC Ensembl
Innerchr6:38133392..38294178hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38160787
hg19160787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115642
Supporting Variants
Samplessample318
Known GenesBTBD9
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14082933
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