A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039420



Internal ID18781951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34378314..34582282hg38UCSC Ensembl
Innerchr15:34670515..34874483hg19UCSC Ensembl
Innerchr15:32457807..32661775hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38203969
hg19203969
hg18203969
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2550n100
Supporting Variantsnssv3547879
Samples
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039420
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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