A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590973



Internal ID16378382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:90259908..90331937hg38UCSC Ensembl
Innerchr3:90309058..90381087hg19UCSC Ensembl
Innerchr3:90391748..90463777hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3872030
hg1972030
hg1872030
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8440n54
Supporting Variantsnssv967758
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590973
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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