A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100869



Internal ID22010102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29041959..29058328hg38UCSC Ensembl
chr19:29532866..29549235hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3816370
hg1916370
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17629309
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100869
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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