A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6336n223



Internal ID22809304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99472230..99473536hg38UCSC Ensembl
chr6:99920106..99921412hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg381307
hg191307
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6568932, nsv6555783
Samples
Known GenesUSP45
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6336n223
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