A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14452013



Internal ID22246978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186654333..186654333hg38UCSC Ensembl
chr3:186372122..186372122hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg386029
hg196029
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3556279
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsInsertion of a L1HS mobile element relative to the reference
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14452013
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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