A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3197326



Internal ID22347224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63138404..63138504hg38UCSC Ensembl
chr18:60805637..60805737hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14448593
SamplesHG00733
Known GenesBCL2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3197326
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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