A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256898



Internal ID21398861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123978962..123991190hg38UCSC Ensembl
chr9:126741241..126753469hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3812229
hg1912229
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730047
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256898
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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