A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590608



Internal ID16031331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:71753743..71754823hg38UCSC Ensembl
Innerchr3:71802894..71803974hg19UCSC Ensembl
Innerchr3:71885584..71886664hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381081
hg191081
hg181081
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8374n54
Supporting Variantsnssv965552
Samples
Known GenesEIF4E3, GPR27
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590608
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