A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978351



Internal ID22753286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1357434..1358162hg38UCSC Ensembl
chr20:1338078..1338806hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38729
hg19729
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398212
Samples
Known GenesFKBP1A-SDCBP2, SDCBP2-AS1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978351
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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