A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589278



Internal ID16376687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:189181..191786hg38UCSC Ensembl
Innerchr3:230864..233469hg19UCSC Ensembl
Innerchr3:205864..208469hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg382606
hg192606
hg182606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8148n54
Supporting Variantsnssv957787
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589278
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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