A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17844743



Internal ID22028386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26664157..26664157hg38UCSC Ensembl
chr13:27238294..27238294hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6248827
Supporting Variants
Samples
Known GenesWASF3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17844743
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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