A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528308



Internal ID15455601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:39755009..39816496hg38UCSC Ensembl
Innerchr4:39756629..39818116hg19UCSC Ensembl
Innerchr4:39433024..39494511hg18UCSC Ensembl
Innerchr4:39579195..39640682hg17UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3861488
hg1961488
hg1861488
hg1761488
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704886
Samples
Known GenesUBE2K
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528308
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