A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199891



Internal ID22349416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29736945..29737023hg38UCSC Ensembl
chr19:30227852..30227930hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14456987
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199891
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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