A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590607



Internal ID16031330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:71753521..71754987hg38UCSC Ensembl
Innerchr3:71802672..71804138hg19UCSC Ensembl
Innerchr3:71885362..71886828hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381467
hg191467
hg181467
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8374n54
Supporting Variantsnssv965551, nssv965550
Samples
Known GenesEIF4E3, GPR27
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590607
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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