A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225488



Internal ID20792528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:28404861..28405834hg38UCSC Ensembl
chr14:28874067..28875040hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38974
hg19974
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590207
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225488
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