A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256390



Internal ID21398413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123979051..123993726hg38UCSC Ensembl
chr9:126741330..126756005hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3814676
hg1914676
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730047
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256390
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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