A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520093



Internal ID15100700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6528168..6540333hg38UCSC Ensembl
Innerchr16:6578169..6590334hg19UCSC Ensembl
Innerchr16:6518170..6530335hg18UCSC Ensembl
Innerchr16:6518170..6530335hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3812166
hg1912166
hg1812166
hg1712166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697220
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520093
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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