A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3209833



Internal ID22357849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:56044510..56044813hg38UCSC Ensembl
chr18:53711741..53712044hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14447428
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)nsv3209833
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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