A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17684637



Internal ID108303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:115271403..115271406hg38UCSC Ensembl
chr12:115709208..115709211hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg386019
hg196019
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560147
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17684637
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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