A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891351



Internal ID18839061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15548450..15554099hg38UCSC Ensembl
Outerchr8:15548450..15554099hg38UCSC Ensembl
Innerchr8:15405959..15411608hg19UCSC Ensembl
Outerchr8:15405959..15411608hg19UCSC Ensembl
Innerchr8:15450330..15455979hg18UCSC Ensembl
Outerchr8:15450330..15455979hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg385650
hg195650
hg185650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780508, essv25780690, essv25779928, essv25785568, essv25784073, essv25783912, essv25782511, essv25780019, essv25798776, essv25786394, essv25779817, essv25799469, essv25785122, essv25782856
Samples
Known GenesTUSC3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891351
Frequency
Sample Size3017
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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