A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523366



Internal ID15450659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:12512312..12526190hg38UCSC Ensembl
Innerchr12:12665246..12679124hg19UCSC Ensembl
Innerchr12:12556513..12570391hg18UCSC Ensembl
Innerchr12:12556513..12570391hg17UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3813879
hg1913879
hg1813879
hg1713879
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699115
Samples
Known GenesDUSP16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523366
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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