A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528564



Internal ID15109171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6574362..6583079hg38UCSC Ensembl
Innerchr16:6624363..6633080hg19UCSC Ensembl
Innerchr16:6564364..6573081hg18UCSC Ensembl
Innerchr16:6564364..6573081hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg388718
hg198718
hg188718
hg178718
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705180
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528564
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer