A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213865



Internal ID22360675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9616370..9641963hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3825594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14407892
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213865
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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