A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592076



Internal ID16379485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:154019385..154028482hg38UCSC Ensembl
Innerchr3:153737174..153746271hg19UCSC Ensembl
Innerchr3:155219864..155228961hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg389098
hg199098
hg189098
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv976852
Samples
Known GenesARHGEF26-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592076
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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