A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17366160



Internal ID22591829
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 StatusS
Merged Variantsnsv5973907
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17366160
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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