A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17855255



Internal ID22038898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172166018..172166018hg38UCSC Ensembl
chr3:171883808..171883808hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6259991
Supporting Variants
Samples
Known GenesFNDC3B
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17855255
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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