A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3410928



Internal ID15257888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3261761..3261780hg38UCSC Ensembl
Innerchr20:3261757..3261784hg38UCSC Ensembl
Outerchr20:3261738..3261803hg38UCSC Ensembl
chr20:3242407..3242426hg19UCSC Ensembl
Innerchr20:3242403..3242430hg19UCSC Ensembl
Outerchr20:3242384..3242449hg19UCSC Ensembl
chr20:3190407..3190426hg18UCSC Ensembl
Innerchr20:3190430..3190403hg18UCSC Ensembl
Outerchr20:3190384..3190449hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9678336, essv9678313, essv9678324
SamplesNA12815, NA12872, NA11840
Known GenesC20orf194
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3410928
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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