A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618150



Internal ID6658345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98344727..98347345hg38UCSC Ensembl
Innerchr8:98344782..98347291hg38UCSC Ensembl
Outerchr8:98344673..98347400hg38UCSC Ensembl
chr8:99356955..99359573hg19UCSC Ensembl
Innerchr8:99357010..99359519hg19UCSC Ensembl
Outerchr8:99356901..99359628hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg382619
hg192619
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13267377, essv13267355, essv13267370, essv13267348, essv13267354, essv13267358, essv13267344, essv13267371, essv13267362, essv13267350, essv13267368, essv13267345, essv13267379, essv13267369, essv13267349, essv13267351, essv13267364, essv13267365, essv13267356, essv13267373, essv13267347, essv13267353, essv13267367, essv13267374, essv13267378, essv13267372, essv13267346, essv13267342, essv13267360, essv13267343, essv13267361, essv13267359, essv13267376, essv13267366, essv13267363, essv13267357, essv13267352, essv13267380, essv13267375
SamplesHG03514, NA19701, HG02944, HG03300, HG03115, HG03100, HG03518, NA18870, NA19107, NA19171, HG02549, NA19138, HG02505, HG02281, HG02420, HG03160, HG02334, NA19152, NA19984, HG03291, HG01077, NA18910, NA19042, HG02283, HG03571, NA19225, HG03354, HG03109, NA19436, NA19035, NA19434, HG02308, NA19454, HG02941, NA19117, HG03157, NA19030, NA19153, HG03166
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618150
Frequency
Sample Size2504
Observed Gain0
Observed Loss39
Observed Complex0
Frequencyn/a


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