A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443893



Internal ID22110074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108991549..108991549hg38UCSC Ensembl
chr13:109643897..109643897hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761921
Samples
Known GenesMYO16
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443893
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer