A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17845155



Internal ID22028798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32463938..32463938hg38UCSC Ensembl
chr13:33038075..33038075hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6248879
Supporting Variants
Samples
Known GenesN4BP2L2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17845155
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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