A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862011



Internal ID22636946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98460878..98478248hg38UCSC Ensembl
chr13:99113132..99130502hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3817371
hg1917371
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455153
Samples
Known GenesSTK24
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862011
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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