A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3287222



Internal ID22385623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113453346..113453466hg38UCSC Ensembl
chr9:116215626..116215746hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14439871
SamplesHG00733
Known GenesRGS3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3287222
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer