A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107730



Internal ID22016963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166070299..166079058hg38UCSC Ensembl
chr6:166483787..166492546hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg388760
hg198760
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558665
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107730
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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