A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14433215



Internal ID22176138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16257438..16261119hg38UCSC Ensembl
chr20:16238083..16241764hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg383682
hg193682
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3191989
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)nssv14433215
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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