A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17855073



Internal ID22038716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:13046163..13046163hg38UCSC Ensembl
chr4:13047787..13047787hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6243758
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17855073
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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