A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569204



Internal ID16009927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:38324444..38371566hg38UCSC Ensembl
Innerchr15:38616645..38663767hg19UCSC Ensembl
Innerchr15:36403937..36451059hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3847123
hg1947123
hg1847123
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv840705
Samples
Known GenesSPRED1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569204
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer