A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645543



Internal ID7032292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24170836..24172150hg38UCSC Ensembl
Innerchr20:24170868..24172119hg38UCSC Ensembl
Outerchr20:24170805..24172182hg38UCSC Ensembl
chr20:24151472..24152786hg19UCSC Ensembl
Innerchr20:24151504..24152755hg19UCSC Ensembl
Outerchr20:24151441..24152818hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg381315
hg191315
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16163906
SamplesHG01920
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645543
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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