A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257398



Internal ID21400818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123977744..123993326hg38UCSC Ensembl
chr9:126740023..126755605hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3815583
hg1915583
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730047
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257398
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