A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589504



Internal ID16376913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:5573343..5860611hg38UCSC Ensembl
Innerchr3:5615030..5902298hg19UCSC Ensembl
Innerchr3:5590030..5877298hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38287269
hg19287269
hg18287269
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv958258
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589504
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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