A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3193027



Internal ID22343526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:8680758..8680854hg38UCSC Ensembl
chr21:9569591..9569687hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5421n152
Supporting Variantsnssv14407881
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)nsv3193027
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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