A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3716325



Internal ID18667920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32217659..33822829hg38UCSC Ensembl
Innerchr16:32228980..33625296hg19UCSC Ensembl
Innerchr16:32136481..33532797hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381605171
hg191396317
hg181396317
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060933
Supporting Variants
Samples
Known GenesLOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3716325
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer