A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17397935



Internal ID22455805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43844633..43867523hg38UCSC Ensembl
chr21:45264514..45287404hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3822891
hg1922891
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968284
Supporting Variants
Samples
Known GenesAGPAT3
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17397935
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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