A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788423



Internal ID18828698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101670768..101810394hg38UCSC Ensembl
Innerchr15:102210971..102350597hg19UCSC Ensembl
Innerchr15:100028494..100168120hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38139627
hg19139627
hg18139627
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892749
Supporting Variants
Samples
Known GenesOR4F6, TARSL2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=19
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788423
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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