A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862492



Internal ID22637427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98475945..98482549hg38UCSC Ensembl
chr13:99128199..99134803hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg386605
hg196605
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458050
Samples
Known GenesSTK24
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862492
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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