A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263628



Internal ID20830668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:120794725..120795818hg38UCSC Ensembl
chr4:121715880..121716973hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg381094
hg191094
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570052
Supporting Variants
Samples
Known GenesPRDM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263628
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