A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14421757



Internal ID22159978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11814071..11820285hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg386215
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3198110
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)nssv14421757
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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