A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3197863



Internal ID22347687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88199978..88211106hg38UCSC Ensembl
chr9:90814893..90826021hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3811129
hg1911129
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9650n152
Supporting Variantsnssv14464780
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)nsv3197863
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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