A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16922033



Internal ID15451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:191716747..191716798hg38UCSC Ensembl
chr2:192581473..192581524hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5398520
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16922033
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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