A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578829



Internal ID20951900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24386708..24387109hg38UCSC Ensembl
chr18:21966672..21967073hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246815
Samples
Known GenesOSBPL1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578829
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