A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610542



Internal ID16051265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15545427..15551464hg38UCSC Ensembl
Innerchr8:15402936..15408973hg19UCSC Ensembl
Innerchr8:15447307..15453344hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg386038
hg196038
hg186038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12015n54
Supporting Variantsnssv1106908
Samples
Known GenesTUSC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610542
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