A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519616



Internal ID15446909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:79998634..80001835hg38UCSC Ensembl
Innerchr16:80032531..80035732hg19UCSC Ensembl
Innerchr16:78590032..78593233hg18UCSC Ensembl
Innerchr16:78590032..78593233hg17UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg383202
hg193202
hg183202
hg173202
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv660588, nssv674875, nssv671371, nssv657072, nssv673162, nssv693008
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519616
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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