A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520915



Internal ID15448208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:21942429..21952245hg38UCSC Ensembl
Innerchr14:22410620..22420469hg19UCSC Ensembl
Innerchr14:21480460..21490309hg18UCSC Ensembl
Innerchr14:21480460..21490309hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg389817
hg199850
hg189850
hg179850
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv689080, nssv677639
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520915
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer