A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046889



Internal ID19136108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:97228851..97290410hg38UCSC Ensembl
Innerchr15:97772081..97833640hg19UCSC Ensembl
Innerchr15:95573085..95634644hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3861560
hg1961560
hg1861560
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3718215
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)nsv1046889
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