A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14422772



Internal ID22161474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27859944..27859944hg38UCSC Ensembl
chr22:28255932..28255932hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3524145
Supporting Variants
SamplesHG00514
Known GenesPITPNB
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsInsertion of a AluY mobile element relative to the reference
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14422772
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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