A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079296



Internal ID21988529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:77455265..77455265hg38UCSC Ensembl
chr8:78367501..78367501hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595078
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079296
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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