A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589508



Internal ID16376917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:5827704..6395186hg38UCSC Ensembl
Innerchr3:5869391..6436873hg19UCSC Ensembl
Innerchr3:5844391..6411873hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38567483
hg19567483
hg18567483
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152474
Samples1780862109_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589508
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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