A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610714



Internal ID16398123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18119721..18136140hg38UCSC Ensembl
Innerchr8:17977230..17993649hg19UCSC Ensembl
Innerchr8:18021510..18037929hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3816420
hg1916420
hg1816420
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1107409
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610714
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