A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227386



Internal ID20794426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22908697..22910205hg38UCSC Ensembl
chr14:23377906..23379414hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381509
hg191509
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580468
Supporting Variants
Samples
Known GenesRBM23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227386
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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