A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616623



Internal ID6656819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23102125..23111473hg38UCSC Ensembl
Innerchr8:23102175..23111423hg38UCSC Ensembl
Outerchr8:23102036..23111562hg38UCSC Ensembl
chr8:22959638..22968986hg19UCSC Ensembl
Innerchr8:22959688..22968936hg19UCSC Ensembl
Outerchr8:22959549..22969075hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg389349
hg199349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13134488
SamplesHG01679
Known GenesLOC254896, TNFRSF10C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616623
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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