A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258237



Internal ID21398626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123979518..123991110hg38UCSC Ensembl
chr9:126741797..126753389hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3811593
hg1911593
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730047
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258237
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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