A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090733



Internal ID21999966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:35861776..35861776hg38UCSC Ensembl
chr13:36435913..36435913hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604068
Samples
Known GenesDCLK1, MIR548F5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090733
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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