A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671303



Internal ID21619608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:16213961..16437498hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38223538
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128548
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671303
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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