A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519868



Internal ID15447161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55597123..55607701hg38UCSC Ensembl
Innerchr16:55631035..55641613hg19UCSC Ensembl
Innerchr16:54188536..54199114hg18UCSC Ensembl
Innerchr16:54188536..54199114hg17UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3810579
hg1910579
hg1810579
hg1710579
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697093
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519868
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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