A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520894



Internal ID15448187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:80008909..80016373hg38UCSC Ensembl
Innerchr16:80042806..80050270hg19UCSC Ensembl
Innerchr16:78600307..78607771hg18UCSC Ensembl
Innerchr16:78600307..78607771hg17UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg387465
hg197465
hg187465
hg177465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv691905, nssv690676, nssv677089
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520894
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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