A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206684



Internal ID22355193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88545931..88548807hg38UCSC Ensembl
chr16:88612339..88615215hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg382877
hg192877
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3337n152
Supporting Variantsnssv14431217, nssv14431218
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206684
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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