A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230250



Internal ID20797290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20465877..20466454hg38UCSC Ensembl
chr14:20934036..20934613hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38578
hg19578
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585461
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230250
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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