A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618294



Internal ID7005176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105911429..105959389hg38UCSC Ensembl
Innerchr8:105911462..105959356hg38UCSC Ensembl
Outerchr8:105911396..105959422hg38UCSC Ensembl
chr8:106923657..106971617hg19UCSC Ensembl
Innerchr8:106923690..106971584hg19UCSC Ensembl
Outerchr8:106923624..106971650hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3847961
hg1947961
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13275071
SamplesHG03160
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618294
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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