A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589862



Internal ID16377271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:20389440..20461637hg38UCSC Ensembl
Innerchr3:20430932..20503129hg19UCSC Ensembl
Innerchr3:20405936..20478133hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3872198
hg1972198
hg1872198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8251n54
Supporting Variantsnssv959882, nssv959883
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589862
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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