A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667666



Internal ID21615971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103197097..103205603hg38UCSC Ensembl
chr10:104956854..104965360hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg388507
hg198507
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068472
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667666
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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