A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3198252



Internal ID22347999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101358929..101368484hg38UCSC Ensembl
chr9:104121211..104130766hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg389556
hg199556
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14465312
SamplesHG00733
Known GenesBAAT
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3198252
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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