A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3523765



Internal ID22393193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26601646..26601646hg38UCSC Ensembl
chr22:26997610..26997610hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14396139
SamplesNA19240
Known GenesCRYBB1
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)nsv3523765
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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