A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14449462



Internal ID22221848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39662711..39662829hg38UCSC Ensembl
chr20:38291353..38291471hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3194470
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14449462
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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