A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17011389



Internal ID75246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54726787..54726787hg38UCSC Ensembl
chr8:55639347..55639347hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5405834
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17011389
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.021122


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