A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061304



Internal ID21970537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:89266458..89266458hg38UCSC Ensembl
chr8:90278687..90278687hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594063
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061304
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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