A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16921502



Internal ID15102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:167504547..167504598hg38UCSC Ensembl
chr2:168361057..168361108hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5397101
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16921502
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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