A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970147



Internal ID22745082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3180562..3181950hg38UCSC Ensembl
chr20:3161208..3162596hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381389
hg191389
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17404852
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970147
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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