A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190859



Internal ID22341657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:8989198..8993536hg38UCSC Ensembl
chr21:9828031..9832369hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg384339
hg194339
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14422062
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3190859
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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