A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891480



Internal ID18839190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:128590939..129018760hg38UCSC Ensembl
Outerchr8:128590939..129018760hg38UCSC Ensembl
Innerchr8:129603185..130031006hg19UCSC Ensembl
Outerchr8:129603185..130031006hg19UCSC Ensembl
Innerchr8:129672367..130100188hg18UCSC Ensembl
Outerchr8:129672367..130100188hg18UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38427822
hg19427822
hg18427822
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789885
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891480
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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