A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616407



Internal ID6656604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:15544186..15580033hg38UCSC Ensembl
Innerchr8:15544186..15580033hg38UCSC Ensembl
Outerchr8:15544069..15580188hg38UCSC Ensembl
chr8:15401695..15437542hg19UCSC Ensembl
Innerchr8:15401695..15437542hg19UCSC Ensembl
Outerchr8:15401578..15437697hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3835848
hg1935848
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13118048, essv13118047, essv13118046, essv13118045
SamplesHG02026, HG02164, HG00584, NA12234
Known GenesTUSC3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616407
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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