A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521142



Internal ID15448435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:63248176..63369038hg38UCSC Ensembl
Innerchr16:63282080..63402942hg19UCSC Ensembl
Innerchr16:61839581..61960443hg18UCSC Ensembl
Innerchr16:61839581..61960443hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38120863
hg19120863
hg18120863
hg17120863
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv685839, nssv682878, nssv692374
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521142
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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