A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593378



Internal ID20966449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23504398..23504589hg38UCSC Ensembl
chr14:23973607..23973798hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235415
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593378
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