A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969274



Internal ID22744209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105764038..105982494hg38UCSC Ensembl
chr9:108526319..108744775hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38218457
hg19218457
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440933
Samples
Known GenesTMEM38B
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969274
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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