A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618402



Internal ID7005284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:110620353..110651271hg38UCSC Ensembl
Innerchr8:110620362..110651263hg38UCSC Ensembl
Outerchr8:110620345..110651280hg38UCSC Ensembl
chr8:111632582..111663500hg19UCSC Ensembl
Innerchr8:111632591..111663492hg19UCSC Ensembl
Outerchr8:111632574..111663509hg19UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg3830919
hg1930919
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1411e214
Supporting Variantsessv13285707
SamplesHG03295
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618402
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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