A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14410184



Internal ID22288155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50021882..50021942hg38UCSC Ensembl
chr22:50460311..50460371hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3201009
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14410184
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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