A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3521812



Internal ID22391228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:60614220..60614220hg38UCSC Ensembl
chr8:61526779..61526779hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14456464
SamplesHG00733
Known GenesRAB2A
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)nsv3521812
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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