A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3198767



Internal ID22348454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59779015..59779072hg38UCSC Ensembl
chr18:57446247..57446304hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14406776
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3198767
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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