A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17845154



Internal ID22028797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32414650..32414650hg38UCSC Ensembl
chr13:32988787..32988787hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6248878
Supporting Variants
Samples
Known GenesN4BP2L1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17845154
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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