A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972126



Internal ID22747061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116855840..116857985hg38UCSC Ensembl
chr11:116726556..116728701hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382146
hg192146
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360919
Samples
Known GenesSIK3
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972126
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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