A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645716



Internal ID7032465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35581450..35585184hg38UCSC Ensembl
Innerchr20:35581451..35585184hg38UCSC Ensembl
Outerchr20:35581450..35585185hg38UCSC Ensembl
chr20:34169372..34173106hg19UCSC Ensembl
Innerchr20:34169373..34173106hg19UCSC Ensembl
Outerchr20:34169372..34173107hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg383735
hg193735
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16179367, essv16179393, essv16179360, essv16179380, essv16179376, essv16179394, essv16179369, essv16179377, essv16179358, essv16179379, essv16179372, essv16179359, essv16179362, essv16179386, essv16179385, essv16179382, essv16179387, essv16179374, essv16179366, essv16179370, essv16179368, essv16179375, essv16179388, essv16179390, essv16179383, essv16179364, essv16179392, essv16179381, essv16179389, essv16179373, essv16179363, essv16179378, essv16179384, essv16179361, essv16179371, essv16179365, essv16179391
SamplesHG00442, HG02250, NA18947, NA18561, NA18545, HG01802, HG00449, NA18995, HG01853, HG00590, HG00867, HG02187, NA18966, NA18954, HG02409, HG00675, NA18645, NA18613, HG00557, HG02380, NA18956, HG02397, HG01810, HG00583, NA18630, NA18531, HG00410, HG01858, NA18632, HG00476, NA19010, HG01862, HG02373, HG00446, HG01872, NA19004, NA18965
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645716
Frequency
Sample Size2504
Observed Gain0
Observed Loss37
Observed Complex0
Frequencyn/a


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