A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568866



Internal ID16009589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32159287..32569140hg38UCSC Ensembl
Innerchr15:32451488..32861341hg19UCSC Ensembl
Innerchr15:30238780..30648633hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38409854
hg19409854
hg18409854
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4446n54
Supporting Variantsnssv839715
Samples
Known GenesCHRNA7, GOLGA8K, GOLGA8O, LOC100996255, ULK4P1, ULK4P2, ULK4P3, WHAMMP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568866
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