A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519368



Internal ID15446661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:68310793..68311133hg38UCSC Ensembl
Innerchr16:68344696..68345036hg19UCSC Ensembl
Innerchr16:66902197..66902537hg18UCSC Ensembl
Innerchr16:66902197..66902537hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38341
hg19341
hg18341
hg17341
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696814
Samples
Known GenesPRMT7, SLC7A6OS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519368
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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