A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589638



Internal ID16377047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8784710..8829531hg38UCSC Ensembl
Innerchr3:8826396..8871216hg19UCSC Ensembl
Innerchr3:8801396..8846216hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3844822
hg1944821
hg1844821
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8215n54
Supporting Variantsnssv958883
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589638
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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