A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859944



Internal ID22634879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45779094..45786396hg38UCSC Ensembl
chr13:46353229..46360531hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg387303
hg197303
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451342
Samples
Known GenesSIAH3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859944
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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