A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589626



Internal ID16377035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8784055..8813413hg38UCSC Ensembl
Innerchr3:8825741..8855099hg19UCSC Ensembl
Innerchr3:8800741..8830099hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3829359
hg1929359
hg1829359
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8214n54
Supporting Variantsnssv958866
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589626
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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