A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645283



Internal ID7032033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:13361737..13370782hg38UCSC Ensembl
Innerchr20:13361737..13370782hg38UCSC Ensembl
Outerchr20:13361237..13371282hg38UCSC Ensembl
chr20:13342384..13351429hg19UCSC Ensembl
Innerchr20:13342384..13351429hg19UCSC Ensembl
Outerchr20:13341884..13351929hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg389046
hg199046
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16143382
SamplesNA18520
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645283
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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