A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561460



Internal ID20934531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:2278671..3813735hg38UCSC Ensembl
chr9:2278671..3813735hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg381535065
hg191535065
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7544n223
Supporting Variantsnssv18280349
Samples
Known GenesFLJ35024, KCNV2, KIAA0020, RFX3, VLDLR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561460
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