A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3209025



Internal ID22357165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:8865262..8865320hg38UCSC Ensembl
chr21:9754095..9754153hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14407883
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)nsv3209025
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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