A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973864



Internal ID22748799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:29104721..29868830hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38764110
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397461
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973864
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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