A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264761



Internal ID20831801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:144425041..144425502hg38UCSC Ensembl
chr4:145346193..145346654hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38462
hg19462
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557475
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264761
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