A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108487



Internal ID22017721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26484815..26511378hg38UCSC Ensembl
chr13:27058952..27085515hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3826564
hg1926564
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610847
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108487
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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