A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13369105



Internal ID4676984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144648618..144659383hg38UCSC Ensembl
Innerchr8:144648638..144659363hg38UCSC Ensembl
Outerchr8:144648598..144659403hg38UCSC Ensembl
chr8:145874003..145884768hg19UCSC Ensembl
Innerchr8:145874023..145884748hg19UCSC Ensembl
Outerchr8:145873983..145884788hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3810766
hg1910766
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619135
Supporting Variants
SamplesHG04202
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13369105
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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