A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893273



Internal ID19184093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:4794039..4801454hg38UCSC Ensembl
Outerchr20:4794039..4801454hg38UCSC Ensembl
Innerchr20:4774685..4782100hg19UCSC Ensembl
Outerchr20:4774685..4782100hg19UCSC Ensembl
Innerchr20:4722685..4730100hg18UCSC Ensembl
Outerchr20:4722685..4730100hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg387416
hg197416
hg187416
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800808
Samples
Known GenesRASSF2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893273
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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