A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17397461



Internal ID22455331
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 StatusS
Merged Variantsnsv5973864
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17397461
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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