A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106086



Internal ID22015319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74269387..74269387hg38UCSC Ensembl
chr18:71936622..71936622hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624978
Samples
Known GenesCYB5A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106086
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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