A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611146



Internal ID16051869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:43203242..43937428hg38UCSC Ensembl
Innerchr8:43058385..43792571hg19UCSC Ensembl
Innerchr8:43177542..43911728hg18UCSC Ensembl
Cytoband8p11.1
Allele length
AssemblyAllele length
hg38734187
hg19734187
hg18734187
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12123n54
Supporting Variantsnssv1113878
Samples
Known GenesPOTEA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611146
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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