A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521819



Internal ID15102426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84350720..84480735hg38UCSC Ensembl
Innerchr16:84384326..84514341hg19UCSC Ensembl
Innerchr16:82941827..83071842hg18UCSC Ensembl
Innerchr16:82941827..83071842hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38130016
hg19130016
hg18130016
hg17130016
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv169n21
Supporting Variantsnssv694590
Samples
Known GenesATP2C2, TLDC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521819
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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