A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3522092



Internal ID22391511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26564035..26564035hg38UCSC Ensembl
chr10:26852964..26852964hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14440219
SamplesHG00733
Known GenesAPBB1IP
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)nsv3522092
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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