A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590673



Internal ID16378082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75400984..75509195hg38UCSC Ensembl
Innerchr3:75450135..75558346hg19UCSC Ensembl
Innerchr3:75532825..75641036hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38108212
hg19108212
hg18108212
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8384n54
Supporting Variantsnssv965694
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590673
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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