A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3520472



Internal ID22389880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28813598..28813598hg38UCSC Ensembl
chr10:29102527..29102527hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14440234, nssv14414526
SamplesHG00733, HG00514
Known Genes
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)nsv3520472
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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