A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3537376



Internal ID22406582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18594293..18594293hg38UCSC Ensembl
chr8:18451803..18451803hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14402204
SamplesNA19240
Known GenesPSD3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3537376
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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