A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520284



Internal ID15447577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:15864299..15878993hg38UCSC Ensembl
Innerchr2:16004423..16019117hg19UCSC Ensembl
Innerchr2:15921874..15936568hg18UCSC Ensembl
Innerchr2:15955021..15969715hg17UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3814695
hg1914695
hg1814695
hg1714695
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694373
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520284
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