A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205808



Internal ID22354444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:8680759..8680854hg38UCSC Ensembl
chr21:9569592..9569687hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5421n152
Supporting Variantsnssv14459595, nssv14432755
SamplesHG00733, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205808
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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