A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6246099



Internal ID22050709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:68638976..68638976hg38UCSC Ensembl
chr8:69551211..69551211hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17840333
Samples
Known GenesC8orf34
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6246099
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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