A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108467



Internal ID22017701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6378333..6387423hg38UCSC Ensembl
chr9:6378333..6387423hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg389091
hg199091
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579359
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108467
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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