A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17845541



Internal ID22029184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98707091..98707091hg38UCSC Ensembl
chr13:99359345..99359345hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6249533
Supporting Variants
Samples
Known GenesSLC15A1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17845541
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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