A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066168



Internal ID18808699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32047162..34150422hg38UCSC Ensembl
Innerchr16:32058483..33952889hg19UCSC Ensembl
Innerchr16:31965984..33860390hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg382103261
hg191894407
hg181894407
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2840n100
Supporting Variantsnssv3549327
Samples
Known GenesHERC2P4, LOC390705, 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)nsv1066168
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