A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16972471



Internal ID49000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:98962011..98962062hg38UCSC Ensembl
chr5:98297715..98297766hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5399833
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16972471
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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