A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645672



Internal ID7032421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32871110..32874183hg38UCSC Ensembl
Innerchr20:32871111..32874182hg38UCSC Ensembl
Outerchr20:32871109..32874184hg38UCSC Ensembl
chr20:31458916..31461989hg19UCSC Ensembl
Innerchr20:31458917..31461988hg19UCSC Ensembl
Outerchr20:31458915..31461990hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg383074
hg193074
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16174914, essv16174907, essv16174917, essv16174910, essv16174903, essv16174916, essv16174908, essv16174915, essv16174902, essv16174913, essv16174909, essv16174905, essv16174904, essv16174911, essv16174906, essv16174912
SamplesNA19701, HG03163, NA19374, HG03369, HG02334, NA18915, HG03428, HG03311, NA18856, NA19712, HG03117, HG01958, NA19376, HG02974, NA19472, NA19093
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645672
Frequency
Sample Size2504
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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