A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666606



Internal ID21614911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132800266..132891417hg38UCSC Ensembl
chr10:134613770..134704921hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3891152
hg1991152
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17069055
Samples
Known GenesTTC40
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666606
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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