A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16898276



Internal ID172991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:228824171..228824171hg38UCSC Ensembl
chr1:228959918..228959918hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5394469
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16898276
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.401187


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