A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581867



Internal ID20954938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75828317..75829463hg38UCSC Ensembl
chr14:76294660..76295806hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381147
hg191147
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2209n223
Supporting Variantsnssv18237476
Samples
Known GenesTTLL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581867
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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