A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528180



Internal ID15108787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:41141146..41186811hg38UCSC Ensembl
Innerchr13:41715282..41760947hg19UCSC Ensembl
Innerchr13:40613282..40658947hg18UCSC Ensembl
Innerchr13:40613282..40658947hg17UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3845666
hg1945666
hg1845666
hg1745666
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704730
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528180
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