A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3549272



Internal ID18500867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32047162..33637917hg38UCSC Ensembl
Innerchr16:32058483..33440384hg19UCSC Ensembl
Innerchr16:31965984..33347885hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381590756
hg191381902
hg181381902
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058780
Supporting Variants
Samples
Known GenesHERC2P4, LOC390705, 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)nssv3549272
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