A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589494



Internal ID18887775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:23082901..23113674hg38UCSC Ensembl
Innerchr3:23124392..23155165hg19UCSC Ensembl
Innerchr3:23099396..23130169hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3830774
hg1930774
hg1830774
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010493
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3589494
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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