A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616686



Internal ID7003572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25647026..25659487hg38UCSC Ensembl
Innerchr8:25647026..25659487hg38UCSC Ensembl
Outerchr8:25646526..25659987hg38UCSC Ensembl
chr8:25504542..25517003hg19UCSC Ensembl
Innerchr8:25504542..25517003hg19UCSC Ensembl
Outerchr8:25504042..25517503hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3812462
hg1912462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13147673
SamplesHG04140
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616686
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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