A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063424



Internal ID18805955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32269023..33801563hg38UCSC Ensembl
Innerchr16:32280344..33604030hg19UCSC Ensembl
Innerchr16:32187845..33511531hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381532541
hg191323687
hg181323687
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2839n100
Supporting Variantsnssv3716344
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)nsv1063424
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