A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780390



Internal ID19170045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:66648103..66920775hg38UCSC Ensembl
Innerchr10:68407861..68680533hg19UCSC Ensembl
Innerchr10:68077867..68350539hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38272673
hg19272673
hg18272673
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891850
Supporting Variants
Samples
Known GenesCTNNA3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=112
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780390
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