A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589406



Internal ID16030129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3972120..4188112hg38UCSC Ensembl
Innerchr3:4013804..4229796hg19UCSC Ensembl
Innerchr3:3988804..4204796hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38215993
hg19215993
hg18215993
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8173n54
Supporting Variantsnssv958003
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589406
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