A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17845791



Internal ID22029434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:26402691..26402691hg38UCSC Ensembl
chr14:26871897..26871897hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6249695
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17845791
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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