A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3523028



Internal ID22392453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119281155..119281155hg38UCSC Ensembl
chr10:121040667..121040667hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14442070
SamplesHG00733
Known GenesGRK5
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)nsv3523028
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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