A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16990518



Internal ID61094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163627509..163627560hg38UCSC Ensembl
chr6:164048541..164048592hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5400499
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16990518
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001873


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