A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780087



Internal ID18820357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133442823..133572278hg38UCSC Ensembl
Innerchr10:135256327..135385782hg19UCSC Ensembl
Innerchr10:135106317..135235772hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38129456
hg19129456
hg18129456
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891902
Supporting Variants
Samples
Known GenesCYP2E1, SCART1, SPRNP1, SYCE1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=63
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780087
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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