A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519892



Internal ID15447185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11915924..11916587hg38UCSC Ensembl
Innerchr16:12009781..12010444hg19UCSC Ensembl
Innerchr16:11917282..11917945hg18UCSC Ensembl
Innerchr16:11917282..11917945hg17UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38664
hg19664
hg18664
hg17664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv659331, nssv661602
Samples
Known GenesGSPT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519892
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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