A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106790



Internal ID22016023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18875033..18930111hg38UCSC Ensembl
chr13:19449173..19504251hg19UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg3855079
hg1955079
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616238
Samples
Known GenesLINC00408
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106790
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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