A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16989621



Internal ID60506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146566158..146566209hg38UCSC Ensembl
chr6:146887294..146887345hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5405870
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16989621
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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