A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3198567



Internal ID22348272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39973436..39976111hg38UCSC Ensembl
chr21:41345363..41348038hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg382676
hg192676
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5532n152
Supporting Variantsnssv14407693, nssv14407694
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)nsv3198567
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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