A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521183



Internal ID15101790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15609148..15690513hg38UCSC Ensembl
Innerchr4:15610771..15692136hg19UCSC Ensembl
Innerchr4:15219869..15301234hg18UCSC Ensembl
Innerchr4:15287040..15368405hg17UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3881366
hg1981366
hg1881366
hg1781366
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv315n21
Supporting Variantsnssv697832
Samples
Known GenesFAM200B, FBXL5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521183
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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