A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3187493



Internal ID22339757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16402652..16405392hg38UCSC Ensembl
chr3:16444159..16446899hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg382741
hg192741
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14462697, nssv14464754
SamplesHG00733
Known GenesRFTN1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3187493
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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