A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971159



Internal ID22746094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172455534..172456235hg38UCSC Ensembl
chr3:172173324..172174025hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426081
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971159
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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