A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058455



Internal ID18800986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32047162..34026275hg38UCSC Ensembl
Innerchr16:32058483..33828742hg19UCSC Ensembl
Innerchr16:31965984..33736243hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381979114
hg191770260
hg181770260
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2840n100
Supporting Variantsnssv3549322, nssv3549324, nssv3549320, nssv3549321, nssv3549323, nssv3549325
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)nsv1058455
Frequency
Sample Size29084
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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