A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3208785



Internal ID22356973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39973495..39976115hg38UCSC Ensembl
chr21:41345422..41348042hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg382621
hg192621
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5532n152
Supporting Variantsnssv14457894, nssv14456197
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)nsv3208785
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer