A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618031



Internal ID7004914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:91780176..91791356hg38UCSC Ensembl
Innerchr8:91780218..91791314hg38UCSC Ensembl
Outerchr8:91780134..91791398hg38UCSC Ensembl
chr8:92792404..92803584hg19UCSC Ensembl
Innerchr8:92792446..92803542hg19UCSC Ensembl
Outerchr8:92792362..92803626hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3811181
hg1911181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13255693
SamplesHG02681
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618031
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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