A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3191142



Internal ID22341891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:998797..998986hg38UCSC Ensembl
chr9:998797..998986hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14429357
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3191142
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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