A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700373



Internal ID15090339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32149331..32647745hg38UCSC Ensembl
Innerchr15:32441532..32939946hg19UCSC Ensembl
Innerchr15:30228824..30727238hg18UCSC Ensembl
Innerchr15:30228824..30727238hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38498415
hg19498415
hg18498415
hg17498415
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517740
Supporting Variants
Samples
Known GenesARHGAP11A, CHRNA7, GOLGA8K, GOLGA8O, GOLGA8R, LOC100996255, SCG5, ULK4P1, ULK4P2, ULK4P3, WHAMMP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700373
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