A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689284



Internal ID15079250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32218309..32222725hg38UCSC Ensembl
Innerchr15:32510510..32514926hg19UCSC Ensembl
Innerchr15:30297802..30302218hg18UCSC Ensembl
Innerchr15:30297802..30302218hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg384417
hg194417
hg184417
hg174417
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517740
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689284
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