A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893812



Internal ID19184632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:90142160..90406830hg38UCSC Ensembl
Outerchr1:90101121..90410331hg38UCSC Ensembl
Innerchr1:90607718..90872387hg19UCSC Ensembl
Outerchr1:90566679..90875888hg19UCSC Ensembl
Innerchr1:90380306..90644975hg18UCSC Ensembl
Outerchr1:90339267..90648476hg18UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38309211
hg19309210
hg18309210
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789797, essv25789826
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893812
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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