A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969677



Internal ID22744612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37817328..37826396hg38UCSC Ensembl
chr9:37817325..37826393hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg389069
hg199069
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442476
Samples
Known GenesDCAF10
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969677
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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