A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263158



Internal ID20830198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138390249..138390970hg38UCSC Ensembl
chr4:139311403..139312124hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38722
hg19722
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561828
Supporting Variants
Samples
Known GenesLINC00499
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263158
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