A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893269



Internal ID19184089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:2477241..2495985hg38UCSC Ensembl
Outerchr20:2477241..2495985hg38UCSC Ensembl
Innerchr20:2457887..2476631hg19UCSC Ensembl
Outerchr20:2457887..2476631hg19UCSC Ensembl
Innerchr20:2405887..2424631hg18UCSC Ensembl
Outerchr20:2405887..2424631hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3818745
hg1918745
hg1818745
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796814
Samples
Known GenesZNF343
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893269
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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