A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617998



Internal ID7004881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90421876..90428878hg38UCSC Ensembl
Innerchr8:90421876..90428878hg38UCSC Ensembl
Outerchr8:90421624..90429126hg38UCSC Ensembl
chr8:91434104..91441106hg19UCSC Ensembl
Innerchr8:91434104..91441106hg19UCSC Ensembl
Outerchr8:91433852..91441354hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg387003
hg197003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13253786, essv13253787
SamplesHG03899, HG03733
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617998
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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