A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220311



Internal ID20787351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21470262..21470849hg38UCSC Ensembl
chr14:21938421..21939008hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595505
Supporting Variants
Samples
Known GenesRAB2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220311
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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