A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524364



Internal ID15104971
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700275
Samples
Known GenesNOB1, NQO1, WWP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524364
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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