A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521817



Internal ID15102424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:34987083..35934461hg38UCSC Ensembl
Innerchr16:34221454..35168832hg19UCSC Ensembl
Innerchr16:34078955..35026333hg18UCSC Ensembl
Innerchr16:34078955..35026333hg17UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38947379
hg19947379
hg18947379
hg17947379
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv165n21
Supporting Variantsnssv694589
Samples
Known GenesFLJ26245, LOC100130700, LOC146481, LOC283914, UBE2MP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521817
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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