A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202167



Internal ID22351367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24872977..24875758hg38UCSC Ensembl
chr16:24884298..24887079hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg382782
hg192782
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3186n152
Supporting Variantsnssv14445932
SamplesHG00733
Known GenesSLC5A11
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202167
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer