A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280352



Internal ID20847392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:22876201..22877129hg38UCSC Ensembl
chr9:22876200..22877128hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38929
hg19929
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555791
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280352
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00024


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