A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201469



Internal ID22350771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137840166..137843552hg38UCSC Ensembl
chr9:140734618..140738004hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg383387
hg193387
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9856n152
Supporting Variantsnssv14389229, nssv14388741
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)nsv3201469
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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