A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280148



Internal ID20847188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135598975..135599520hg38UCSC Ensembl
chr9:138490821..138491366hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38546
hg19546
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559751
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280148
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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