A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14451427



Internal ID22246469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:81941841..81941841hg38UCSC Ensembl
chr3:81990992..81990992hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg386059
hg196059
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3553012
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)nssv14451427
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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