A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17114333



Internal ID21512684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:45059325..45082172hg38UCSC Ensembl
chr2:45286464..45309311hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3822848
hg1922848
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5669858
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17114333
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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