A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17598174



Internal ID21790218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24583421..24606185hg38UCSC Ensembl
chr14:25052627..25075391hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3822765
hg1922765
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6105513
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17598174
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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