A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268210



Internal ID20835250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:33162555..33441035hg38UCSC Ensembl
chr5:33162661..33441141hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38278481
hg19278481
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574846
Supporting Variants
Samples
Known GenesTARS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268210
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