A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446347



Internal ID22112526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69813824..69813824hg38UCSC Ensembl
chr11:69628592..69628592hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15757193
Samples
Known GenesFGF3
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446347
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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