A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567480



Internal ID20940551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111453698..111454921hg38UCSC Ensembl
chr6:111774901..111776124hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381224
hg191224
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6369n223
Supporting Variantsnssv18268493
Samples
Known GenesREV3L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567480
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