A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589431



Internal ID16030154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4093768..4198269hg38UCSC Ensembl
Innerchr3:4135452..4239953hg19UCSC Ensembl
Innerchr3:4110452..4214953hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38104502
hg19104502
hg18104502
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8179n54
Supporting Variantsnssv1152456
SamplesHGDP01319
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589431
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