A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893355



Internal ID19184175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61179529..61184733hg38UCSC Ensembl
Outerchr20:61178256..61187161hg38UCSC Ensembl
Innerchr20:59754585..59759789hg19UCSC Ensembl
Outerchr20:59753312..59762217hg19UCSC Ensembl
Innerchr20:59187980..59193184hg18UCSC Ensembl
Outerchr20:59186707..59195612hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg388906
hg198906
hg188906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799284, essv25781398, essv25781768, essv25796381, essv25781039, essv25786126, essv25797690
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893355
Frequency
Sample Size3017
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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