A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592189



Internal ID16379598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162415287..162508329hg38UCSC Ensembl
Innerchr3:162133075..162226117hg19UCSC Ensembl
Innerchr3:163615769..163708811hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3893043
hg1993043
hg1893043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8674n54
Supporting Variantsnssv1152029
SamplesHGDP01304
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592189
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