A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618331



Internal ID7005213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:107515220..107527332hg38UCSC Ensembl
Innerchr8:107515267..107527285hg38UCSC Ensembl
Outerchr8:107515173..107527379hg38UCSC Ensembl
chr8:108527448..108539560hg19UCSC Ensembl
Innerchr8:108527495..108539513hg19UCSC Ensembl
Outerchr8:108527401..108539607hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3812113
hg1912113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13279434
SamplesNA19475
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618331
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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