A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237471



Internal ID20804511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75755094..75756675hg38UCSC Ensembl
chr14:76221437..76223018hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381582
hg191582
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588453
Supporting Variants
Samples
Known GenesTTLL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237471
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer