A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669184



Internal ID21617489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:227492704..227508429hg38UCSC Ensembl
chr1:227680405..227696130hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg3815726
hg1915726
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17062886
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669184
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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