A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589966



Internal ID16377375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26004870..26144282hg38UCSC Ensembl
Innerchr3:26046361..26185773hg19UCSC Ensembl
Innerchr3:26021365..26160777hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38139413
hg19139413
hg18139413
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8265n54
Supporting Variantsnssv960142
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589966
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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