A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616204



Internal ID7003091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9863400..9869174hg38UCSC Ensembl
Innerchr8:9863900..9868674hg38UCSC Ensembl
Outerchr8:9862400..9870174hg38UCSC Ensembl
chr8:9720910..9726684hg19UCSC Ensembl
Innerchr8:9721410..9726184hg19UCSC Ensembl
Outerchr8:9719910..9727684hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg385775
hg195775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13099237, essv13099235, essv13099236
SamplesNA18563, NA18539, HG02047
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616204
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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