A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17845046



Internal ID22028689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76717416..76717416hg38UCSC Ensembl
chr13:77291551..77291551hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6249318
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17845046
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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