A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17855254



Internal ID22038897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172139728..172139728hg38UCSC Ensembl
chr3:171857518..171857518hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6259990
Supporting Variants
Samples
Known GenesFNDC3B
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17855254
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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