A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590116



Internal ID16377525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41052084..41103204hg38UCSC Ensembl
Innerchr3:41093575..41144695hg19UCSC Ensembl
Innerchr3:41068579..41119699hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3851121
hg1951121
hg1851121
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8288n54
Supporting Variantsnssv962394, nssv962393, nssv962392
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590116
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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