A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266893



Internal ID20833933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:140272230..140273082hg38UCSC Ensembl
chr5:139651815..139652667hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38853
hg19853
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559793
Supporting Variants
Samples
Known GenesPFDN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266893
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