A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577281



Internal ID20950352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:54369491..54370275hg38UCSC Ensembl
chr18:51895861..51896645hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38785
hg19785
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244678
Samples
Known GenesC18orf54
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577281
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