A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967795



Internal ID22742731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107299008..107317191hg38UCSC Ensembl
chr11:107169734..107187917hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3818184
hg1918184
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353325
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967795
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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