A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9650n152



Internal ID22825353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88199974..88211115hg38UCSC Ensembl
chr9:90814889..90826030hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3811142
hg1911142
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3206739, nsv3197863, nsv3197056
SamplesNA19240, HG00733, 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)dgv9650n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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