A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667114



Internal ID21615421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106998285..107006254hg38UCSC Ensembl
chr6:107319489..107327458hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg387970
hg197970
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147708
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667114
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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