A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645089



Internal ID7031840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5058351..5066967hg38UCSC Ensembl
Innerchr20:5058372..5066947hg38UCSC Ensembl
Outerchr20:5058331..5066988hg38UCSC Ensembl
chr20:5038997..5047613hg19UCSC Ensembl
Innerchr20:5039018..5047593hg19UCSC Ensembl
Outerchr20:5038977..5047634hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg388617
hg198617
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16126073
SamplesHG02628
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645089
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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