A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528734



Internal ID15109341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6823787..6898632hg38UCSC Ensembl
Innerchr16:6873788..6948633hg19UCSC Ensembl
Innerchr16:6813789..6888634hg18UCSC Ensembl
Innerchr16:6813789..6888634hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3874846
hg1974846
hg1874846
hg1774846
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705390
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528734
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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