A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561974



Internal ID20935045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:25500711..25506739hg38UCSC Ensembl
chr9:25500709..25506737hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg386029
hg196029
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7659n223
Supporting Variantsnssv18280377
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561974
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