A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3207092



Internal ID22355541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86567018..86567201hg38UCSC Ensembl
chr16:86600624..86600807hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14463977
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)nsv3207092
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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