A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967568



Internal ID22742503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:29649681..30207701hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38558021
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1306n209
Supporting Variantsnssv17403512
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967568
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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