A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078084



Internal ID21987317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:86086770..86086770hg38UCSC Ensembl
chr8:87098999..87098999hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593120
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078084
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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