A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526413



Internal ID15453706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:54584225..54612584hg38UCSC Ensembl
Innerchr15:54876423..54904782hg19UCSC Ensembl
Innerchr15:52663715..52692074hg18UCSC Ensembl
Innerchr15:52663715..52692074hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3828360
hg1928360
hg1828360
hg1728360
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702713
Samples
Known GenesUNC13C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526413
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