A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3198358



Internal ID22348094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35116756..35116808hg38UCSC Ensembl
chr19:35607660..35607712hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4248n152
Supporting Variantsnssv14393518
SamplesNA19240
Known GenesFXYD3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3198358
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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