A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237902



Internal ID20804942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58411262..58411807hg38UCSC Ensembl
chr14:58877980..58878525hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38546
hg19546
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579120
Supporting Variants
Samples
Known GenesTIMM9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237902
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00055


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