A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616187



Internal ID7003074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9501093..9504885hg38UCSC Ensembl
Innerchr8:9501093..9504885hg38UCSC Ensembl
Outerchr8:9500894..9505105hg38UCSC Ensembl
chr8:9358603..9362395hg19UCSC Ensembl
Innerchr8:9358603..9362395hg19UCSC Ensembl
Outerchr8:9358404..9362615hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg383793
hg193793
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13095691
SamplesHG00310
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616187
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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