A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516630



Internal ID15443923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86774069..86794552hg38UCSC Ensembl
Innerchr16:86807675..86828158hg19UCSC Ensembl
Innerchr16:85365176..85385659hg18UCSC Ensembl
Innerchr16:85365176..85385659hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3820484
hg1920484
hg1820484
hg1720484
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv669403, nssv653253
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516630
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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