A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4768216



Internal ID20544076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109655017..109655017hg38UCSC Ensembl
chr13:110307364..110307364hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261431
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4768216
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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