A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752708



Internal ID20528568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:35861692..35861692hg38UCSC Ensembl
chr13:36435829..36435829hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289886
Samples
Known GenesDCLK1, MIR548F5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752708
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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