A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17845024



Internal ID22028667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:74567070..74567070hg38UCSC Ensembl
chr13:75141207..75141207hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6249298
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17845024
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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