A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264894



Internal ID20831934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:164414350..164420210hg38UCSC Ensembl
chr4:165335502..165341362hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg385861
hg195861
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574917
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264894
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