A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3537887



Internal ID22407080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:10572..10572hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38395
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14422954, nssv14451321
SamplesHG00733, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3537887
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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