A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589448



Internal ID16030171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4183047..4304082hg38UCSC Ensembl
Innerchr3:4224731..4345766hg19UCSC Ensembl
Innerchr3:4199731..4320766hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38121036
hg19121036
hg18121036
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8185n54
Supporting Variantsnssv958047
Samples
Known GenesSETMAR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589448
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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