A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016237



Internal ID21925580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11345015..11363234hg38UCSC Ensembl
chr8:11202524..11220743hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3818220
hg1918220
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558303
Samples
Known GenesTDH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016237
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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