A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17709402



Internal ID133068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:48024746..48024797hg38UCSC Ensembl
chr16:48058657..48058708hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg383449
hg193449
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563053
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17709402
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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