A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667916



Internal ID21616222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:47827131..47904924hg38UCSC Ensembl
chr20:46455875..46533668hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3877794
hg1977794
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117268
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667916
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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