A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106909



Internal ID22016142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:92447888..92468131hg38UCSC Ensembl
chr6:93157606..93177849hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3820244
hg1920244
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564215
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106909
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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