A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17845893



Internal ID22029536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:52437397..52437397hg38UCSC Ensembl
chr14:52904115..52904115hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6258869
Supporting Variants
Samples
Known GenesTXNDC16
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17845893
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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