A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192354



Internal ID22342954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10129144..10129227hg38UCSC Ensembl
chr21:10607172..10607255hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5438n152
Supporting Variantsnssv14449606
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192354
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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