A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893279



Internal ID18837413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:7587317..7893171hg38UCSC Ensembl
Outerchr20:7582024..7999743hg38UCSC Ensembl
Innerchr20:7567964..7873818hg19UCSC Ensembl
Outerchr20:7562671..7980390hg19UCSC Ensembl
Innerchr20:7515964..7821818hg18UCSC Ensembl
Outerchr20:7510671..7928390hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38417720
hg19417720
hg18417720
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787842, essv25792862, essv25791514, essv25790819
Samples
Known GenesHAO1, TMX4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893279
Frequency
Sample Size3017
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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