A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854261



Internal ID22037904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:165018098..165018098hg38UCSC Ensembl
chr3:164735886..164735886hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38254
hg19254
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6259907
Supporting Variants
Samples
Known GenesSI
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854261
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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