A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446721



Internal ID22112899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78879008..78879008hg38UCSC Ensembl
chr11:78590053..78590053hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38715
hg19715
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761225
Samples
Known GenesTENM4
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446721
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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