A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569508



Internal ID16356917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:54584014..54612584hg38UCSC Ensembl
Innerchr15:54876212..54904782hg19UCSC Ensembl
Innerchr15:52663504..52692074hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3828571
hg1928571
hg1828571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv843298
Samples
Known GenesUNC13C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569508
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