A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584171



Internal ID20957242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40180668..40182022hg38UCSC Ensembl
chr15:40472869..40474223hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381355
hg191355
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238018
Samples
Known GenesBUB1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584171
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