A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590493



Internal ID20963564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42830331..42830732hg38UCSC Ensembl
chr15:43122529..43122930hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239024
Samples
Known GenesTTBK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590493
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