A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3198579



Internal ID22348283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9810733..9840509hg38UCSC Ensembl
chr4_gl000193_random:78047..107823hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3829777
hg1929777
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14432774
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)nsv3198579
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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