A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973907



Internal ID22748842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110256049..110256469hg38UCSC Ensembl
chr12:110693854..110694274hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38421
hg19421
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366160
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973907
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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