A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854979



Internal ID22038622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167446531..167446531hg38UCSC Ensembl
chr3:167164319..167164319hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6259932
Supporting Variants
Samples
Known GenesSERPINI2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854979
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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