A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703956



Internal ID127622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69290335..69290386hg38UCSC Ensembl
chr15:69582674..69582725hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416804
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703956
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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