A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3188203



Internal ID22340131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165081465..165083902hg38UCSC Ensembl
chr4:166002617..166005054hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg382438
hg192438
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6934n152
Supporting Variantsnssv14410449
SamplesNA19240
Known GenesTMEM192
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3188203
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