A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589433



Internal ID16030156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4102189..4140066hg38UCSC Ensembl
Innerchr3:4143873..4181750hg19UCSC Ensembl
Innerchr3:4118873..4156750hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3837878
hg1937878
hg1837878
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8181n54
Supporting Variantsnssv958031
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589433
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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