A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3209449



Internal ID22357527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107388992..107389044hg38UCSC Ensembl
chr9:110151273..110151325hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14428882, nssv14460180
SamplesHG00733, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3209449
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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