A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861141



Internal ID22636076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98442294..98451594hg38UCSC Ensembl
chr13:99094548..99103848hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg389301
hg199301
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458832
Samples
Known GenesFARP1, STK24
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861141
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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