A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617978



Internal ID6658173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:89418010..89579892hg38UCSC Ensembl
chr8:90430239..90592121hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38161883
hg19161883
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13252060, essv13252059
SamplesNA19795, NA18988
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617978
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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