A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569694



Internal ID16357103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:63189850..63190545hg38UCSC Ensembl
Innerchr15:63482049..63482744hg19UCSC Ensembl
Innerchr15:61269102..61269797hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38696
hg19696
hg18696
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4570n54
Supporting Variantsnssv843960, nssv843959, nssv843958
Samples
Known GenesRAB8B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569694
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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