A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279868



Internal ID20846908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125166713..125167417hg38UCSC Ensembl
chr9:127928992..127929696hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38705
hg19705
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569300
Supporting Variants
Samples
Known GenesPPP6C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279868
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer