A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859349



Internal ID22634284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99428936..99430341hg38UCSC Ensembl
chr13:100081190..100082595hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg381406
hg191406
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468273, nssv17468083
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859349
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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