A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590667



Internal ID16378076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75397370..75566248hg38UCSC Ensembl
Innerchr3:75446521..75615399hg19UCSC Ensembl
Innerchr3:75529211..75698089hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38168879
hg19168879
hg18168879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8382n54
Supporting Variantsnssv965678
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590667
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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