A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577709



Internal ID20950780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40208539..40208965hg38UCSC Ensembl
chr15:40500740..40501166hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38427
hg19427
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238021
Samples
Known GenesBUB1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577709
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