A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671035



Internal ID21619340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79817675..79845180hg38UCSC Ensembl
chr13:80391810..80419315hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3827506
hg1927506
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081528
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671035
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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