A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860215



Internal ID22635150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:104839792..104840838hg38UCSC Ensembl
chr13:105492143..105493189hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg381047
hg191047
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469246, nssv17454760
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860215
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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