A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14418429



Internal ID22155090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86024255..86024255hg38UCSC Ensembl
chr16:86057861..86057861hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3546945
Supporting Variants
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14418429
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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