A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968317



Internal ID22743253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:29592488..30264094hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38671607
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1306n209
Supporting Variantsnssv17389759
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968317
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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