A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266876



Internal ID20833916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139610462..139611367hg38UCSC Ensembl
chr5:138990047..138990952hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38906
hg19906
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557727
Supporting Variants
Samples
Known GenesUBE2D2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266876
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