A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572272



Internal ID20945343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125162190..125164483hg38UCSC Ensembl
chr9:127924469..127926762hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg382294
hg192294
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279866
Samples
Known GenesPPP6C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572272
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