A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109997



Internal ID22019230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113111687..113112887hg38UCSC Ensembl
chr9:115873967..115875167hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381201
hg191201
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578904
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109997
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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