A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526651



Internal ID15453944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3415368..3626211hg38UCSC Ensembl
Innerchr3:3457052..3667895hg19UCSC Ensembl
Innerchr3:3432052..3642895hg18UCSC Ensembl
Innerchr3:3432052..3642895hg17UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38210844
hg19210844
hg18210844
hg17210844
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702978
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526651
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