A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3207192



Internal ID22355622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123119104..123119199hg38UCSC Ensembl
chr9:125881383..125881478hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14428941
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)nsv3207192
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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