A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589880



Internal ID16377289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21041604..21103109hg38UCSC Ensembl
Innerchr3:21083096..21144601hg19UCSC Ensembl
Innerchr3:21058100..21119605hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3861506
hg1961506
hg1861506
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv959899
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589880
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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