A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519064



Internal ID15446357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89913086..89919746hg38UCSC Ensembl
Innerchr16:89979494..89986154hg19UCSC Ensembl
Innerchr16:88506995..88513655hg18UCSC Ensembl
Innerchr16:88506995..88513655hg17UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg386661
hg196661
hg186661
hg176661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696536
Samples
Known GenesMC1R
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519064
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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