A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977098



Internal ID52124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:167943568..167943619hg38UCSC Ensembl
chr5:167370573..167370624hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38211
hg19211
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5398771
Supporting Variants
Samples
Known GenesTENM2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977098
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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