A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16892354



Internal ID169099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161019993..161020003hg38UCSC Ensembl
chr1:160989783..160989793hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5412847
Supporting Variants
Samples
Known GenesF11R
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16892354
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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