A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590680



Internal ID16378089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75403949..75491393hg38UCSC Ensembl
Innerchr3:75453100..75540544hg19UCSC Ensembl
Innerchr3:75535790..75623234hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3887445
hg1987445
hg1887445
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8384n54
Supporting Variantsnssv965703, nssv965704
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590680
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer