A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17846369



Internal ID22030012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85535921..85535921hg38UCSC Ensembl
chr14:86002265..86002265hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6241626
Supporting Variants
Samples
Known GenesFLRT2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17846369
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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