A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972087



Internal ID22747022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:11866384..11895926hg38UCSC Ensembl
chr3:11907858..11937400hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3829543
hg1929543
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399144
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972087
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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