A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792107



Internal ID19164792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68106900..68213569hg38UCSC Ensembl
Innerchr10:69866657..69973326hg19UCSC Ensembl
Innerchr10:69536663..69643332hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38106670
hg19106670
hg18106670
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891854
Supporting Variants
Samples
Known GenesMYPN
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=36
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792107
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