A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17845130



Internal ID22028773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29804537..29804537hg38UCSC Ensembl
chr13:30378674..30378674hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6248854
Supporting Variants
Samples
Known GenesUBL3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17845130
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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