A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058089



Internal ID19147308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32938920..34026275hg38UCSC Ensembl
Innerchr16:32950241..33828742hg19UCSC Ensembl
Innerchr16:32857742..33736243hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381087356
hg19878502
hg18878502
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2898n100
Supporting Variantsnssv3717232, nssv3717233, nssv3552067, nssv3552068
Samples
Known GenesLOC390705, RNU6-76P, 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)nsv1058089
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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