A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517512



Internal ID15098119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:68026786..68132927hg38UCSC Ensembl
Innerchr15:68319124..68425265hg19UCSC Ensembl
Innerchr15:66106178..66212319hg18UCSC Ensembl
Innerchr15:66106178..66212319hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38106142
hg19106142
hg18106142
hg17106142
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv665203, nssv652239
Samples
Known GenesPIAS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517512
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