A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589409



Internal ID16030132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4020881..4209187hg38UCSC Ensembl
Innerchr3:4062565..4250871hg19UCSC Ensembl
Innerchr3:4037565..4225871hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38188307
hg19188307
hg18188307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8174n54
Supporting Variantsnssv958005
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589409
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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