A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14418930



Internal ID22155807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:54306777..54306777hg38UCSC Ensembl
chr16:54340689..54340689hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3555720
Supporting Variants
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14418930
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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