A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618151



Internal ID7005034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98376284..98376765hg38UCSC Ensembl
Innerchr8:98376334..98376715hg38UCSC Ensembl
Outerchr8:98376232..98376817hg38UCSC Ensembl
chr8:99388512..99388993hg19UCSC Ensembl
Innerchr8:99388562..99388943hg19UCSC Ensembl
Outerchr8:99388460..99389045hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38482
hg19482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13267382, essv13267381
SamplesNA19921, NA19310
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618151
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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