A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700275



Internal ID15090241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:69711242..69769540hg38UCSC Ensembl
Innerchr16:69745145..69803443hg19UCSC Ensembl
Innerchr16:68302646..68360944hg18UCSC Ensembl
Innerchr16:68302646..68360944hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3858299
hg1958299
hg1858299
hg1758299
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524364
Supporting Variants
Samples
Known GenesNOB1, NQO1, WWP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700275
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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