A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520998



Internal ID15448291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58773638..58800315hg38UCSC Ensembl
Innerchr16:58807542..58834219hg19UCSC Ensembl
Innerchr16:57365043..57391720hg18UCSC Ensembl
Innerchr16:57365043..57391720hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3826678
hg1926678
hg1826678
hg1726678
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv689665, nssv679618
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520998
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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