A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848988



Internal ID22623923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98510875..98519629hg38UCSC Ensembl
chr13:99163129..99171883hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg388755
hg198755
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458269, nssv17466424
Samples
Known GenesSTK24
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848988
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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