A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5398682



Internal ID178077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96428737..96428788hg38UCSC Ensembl
chr8:97440965..97441016hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17016111
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5398682
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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