A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3196068



Internal ID22346145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:581060..581134hg38UCSC Ensembl
chr19:581060..581134hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14392701
SamplesNA19240
Known GenesBSG
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3196068
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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