A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092767



Internal ID21409967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:90117198..90328344hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38211147
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665579
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092767
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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