A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9698n152



Internal ID22825401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104493246..104493375hg38UCSC Ensembl
chr9:107255527..107255656hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3287486, nsv3527418
SamplesNA19238, HG00732, HG00513, HG00514
Known Genes
MethodMerging
Sequencing
AnalysisMultiple analysis algorthms
PhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformIllumina HiSeq
See merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv9698n152
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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