A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519328



Internal ID15446621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:49582530..49583944hg38UCSC Ensembl
Innerchr16:49616441..49617855hg19UCSC Ensembl
Innerchr16:48173942..48175356hg18UCSC Ensembl
Innerchr16:48173942..48175356hg17UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg381415
hg191415
hg181415
hg171415
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696794
Samples
Known GenesZNF423
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519328
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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