A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3717154



Internal ID19015435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32421720..33813659hg38UCSC Ensembl
Innerchr16:32433041..33616126hg19UCSC Ensembl
Innerchr16:32340542..33523627hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381391940
hg191183086
hg181183086
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063358
Supporting Variants
Samples
Known GenesLOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3717154
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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