A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619081



Internal ID7005962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:142219061..142256645hg38UCSC Ensembl
chr8:143300422..143338006hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3837585
hg1937585
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13361825
SamplesNA20514
Known GenesTSNARE1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619081
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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