A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528446



Internal ID15109053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121712516..121715931hg38UCSC Ensembl
Innerchr10:123472030..123475445hg19UCSC Ensembl
Innerchr10:123462020..123465435hg18UCSC Ensembl
Innerchr10:123462020..123465435hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg383416
hg193416
hg183416
hg173416
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705041
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528446
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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