A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978902



Internal ID22753837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17147722..17152166hg38UCSC Ensembl
chr19:17258532..17262976hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg384445
hg194445
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17404594
Samples
Known GenesMYO9B
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978902
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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