A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968734



Internal ID22743669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:6879472..6879883hg38UCSC Ensembl
chr20:6860119..6860530hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38412
hg19412
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389800
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968734
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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