A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3191551



Internal ID22342242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19489073..19489128hg38UCSC Ensembl
chr16:19500395..19500450hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14445904
SamplesHG00733
Known GenesTMC5
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3191551
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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