A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893272



Internal ID19184092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:4282944..4297045hg38UCSC Ensembl
Outerchr20:4282944..4297045hg38UCSC Ensembl
Innerchr20:4263591..4277692hg19UCSC Ensembl
Outerchr20:4263591..4277692hg19UCSC Ensembl
Innerchr20:4211591..4225692hg18UCSC Ensembl
Outerchr20:4211591..4225692hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3814102
hg1914102
hg1814102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786566
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893272
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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