A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16966043



Internal ID44683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55824386..55824437hg38UCSC Ensembl
chr5:55120214..55120265hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5409836
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16966043
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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