A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978604



Internal ID22753540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18586549..18586647hg38UCSC Ensembl
chr20:18567193..18567291hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17406482
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978604
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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