A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893323



Internal ID18837457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23785640..23843219hg38UCSC Ensembl
Outerchr20:23785640..23843219hg38UCSC Ensembl
Innerchr20:23766277..23823856hg19UCSC Ensembl
Outerchr20:23766277..23823856hg19UCSC Ensembl
Innerchr20:23714277..23771856hg18UCSC Ensembl
Outerchr20:23714277..23771856hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3857580
hg1957580
hg1857580
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797191
Samples
Known GenesCST2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893323
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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