A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039450



Internal ID19128669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20364686..20406244hg38UCSC Ensembl
Innerchr15:20569939..20611497hg19UCSC Ensembl
Innerchr15:18829953..18871511hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3841559
hg1941559
hg1841559
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2264n100
Supporting Variantsnssv3537639
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)nsv1039450
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