A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976666



Internal ID22751601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113823058..113831093hg38UCSC Ensembl
chr3:113541905..113549940hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg388036
hg198036
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17405131
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976666
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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