A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591067



Internal ID16378476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:98676373..98693253hg38UCSC Ensembl
Innerchr3:98395217..98412097hg19UCSC Ensembl
Innerchr3:99877907..99894787hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3816881
hg1916881
hg1816881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8459n54
Supporting Variantsnssv968220
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591067
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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