A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15757193



Internal ID22091669
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 StatusS
Merged Variantsnsv4446347
Supporting Variants
Samples
Known GenesFGF3
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15757193
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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