A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616196



Internal ID7003083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9745776..9812993hg38UCSC Ensembl
Innerchr8:9745776..9812993hg38UCSC Ensembl
Outerchr8:9745276..9813493hg38UCSC Ensembl
chr8:9603286..9670503hg19UCSC Ensembl
Innerchr8:9603286..9670503hg19UCSC Ensembl
Outerchr8:9602786..9671003hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3867218
hg1967218
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13097508
SamplesHG02047
Known GenesTNKS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616196
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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