A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17845952



Internal ID22029595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102658057..102658057hg38UCSC Ensembl
chr13:103310407..103310407hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6249560
Supporting Variants
Samples
Known GenesTPP2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17845952
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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