A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526472



Internal ID15107079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6922215..7012444hg38UCSC Ensembl
Innerchr16:6972216..7062445hg19UCSC Ensembl
Innerchr16:6912217..7002446hg18UCSC Ensembl
Innerchr16:6912217..7002446hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3890230
hg1990230
hg1890230
hg1790230
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702777
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526472
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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