A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9680n152



Internal ID22825383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98393369..98393425hg38UCSC Ensembl
chr9:101155651..101155707hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3212457, nsv3222756
SamplesNA19240
Known GenesGABBR2
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)dgv9680n152
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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