A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616839



Internal ID7003725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33641806..33648565hg38UCSC Ensembl
Innerchr8:33641837..33648535hg38UCSC Ensembl
Outerchr8:33641776..33648596hg38UCSC Ensembl
chr8:33499324..33506083hg19UCSC Ensembl
Innerchr8:33499355..33506053hg19UCSC Ensembl
Outerchr8:33499294..33506114hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg386760
hg196760
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13161524, essv13161525
SamplesHG02260, NA19072
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616839
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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