A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559386



Internal ID20932457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112306193..112307417hg38UCSC Ensembl
chr9:115068473..115069697hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381225
hg191225
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279592
Samples
Known GenesMIR3134, PTBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559386
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