A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575986



Internal ID20949057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:27231708..27232318hg38UCSC Ensembl
chr18:24811672..24812282hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38611
hg19611
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243963
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575986
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer