A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016924



Internal ID21926267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33385803..33389917hg38UCSC Ensembl
chr8:33243321..33247435hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg384115
hg194115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571784
Samples
Known GenesFUT10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016924
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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