A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893267



Internal ID19184087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1175210..1181971hg38UCSC Ensembl
Outerchr20:1175210..1181971hg38UCSC Ensembl
Innerchr20:1155854..1162615hg19UCSC Ensembl
Outerchr20:1155854..1162615hg19UCSC Ensembl
Innerchr20:1103854..1110615hg18UCSC Ensembl
Outerchr20:1103854..1110615hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg386762
hg196762
hg186762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799361
Samples
Known GenesTMEM74B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893267
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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