A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238356



Internal ID20805396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93217246..93217981hg38UCSC Ensembl
chr14:93683592..93684327hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg38736
hg19736
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588196
Supporting Variants
Samples
Known GenesUBR7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238356
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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