A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281591



Internal ID20490809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158473771..158473771hg38UCSC Ensembl
chr1:158443561..158443561hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763343
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281591
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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