A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5672482



Internal ID21620787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:48199211..48206661hg38UCSC Ensembl
chr13:48773347..48780797hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg387451
hg197451
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17082932
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5672482
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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