A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222322



Internal ID20789362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101976016..101976364hg38UCSC Ensembl
chr14:102442353..102442701hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588829
Supporting Variants
Samples
Known GenesDYNC1H1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222322
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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