A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14411076



Internal ID22290131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:22050727..22054133hg38UCSC Ensembl
chr6:22050956..22054362hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg383407
hg193407
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3172651
Supporting Variants
SamplesNA19240
Known GenesCASC15
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14411076
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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