A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521597



Internal ID15448890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:114180343..114306059hg38UCSC Ensembl
Innerchr4:115101499..115227215hg19UCSC Ensembl
Innerchr4:115320948..115446664hg18UCSC Ensembl
Innerchr4:115459103..115584819hg17UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38125717
hg19125717
hg18125717
hg17125717
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv327n21
Supporting Variantsnssv698214
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521597
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