A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528698



Internal ID15455991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71568507..71583671hg38UCSC Ensembl
Innerchr15:71860846..71876010hg19UCSC Ensembl
Innerchr15:69647900..69663064hg18UCSC Ensembl
Innerchr15:69647900..69663064hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3815165
hg1915165
hg1815165
hg1715165
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705344
Samples
Known GenesTHSD4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528698
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