A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852666



Internal ID22627601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98526581..98535066hg38UCSC Ensembl
chr13:99178835..99187320hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg388486
hg198486
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460527, nssv17468576
Samples
Known GenesSTK24
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852666
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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