A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3193101



Internal ID22343590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:13936868..13936928hg38UCSC Ensembl
chr19:14047681..14047741hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4146n152
Supporting Variantsnssv14447943
SamplesHG00733
Known GenesPODNL1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3193101
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