A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893277



Internal ID19184097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:5720835..5847729hg38UCSC Ensembl
Outerchr20:5720835..5847729hg38UCSC Ensembl
Innerchr20:5701481..5828375hg19UCSC Ensembl
Outerchr20:5701481..5828375hg19UCSC Ensembl
Innerchr20:5649481..5776375hg18UCSC Ensembl
Outerchr20:5649481..5776375hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38126895
hg19126895
hg18126895
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792716
Samples
Known GenesC20orf196
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893277
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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