A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1018n152



Internal ID22816721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97193181..97193249hg38UCSC Ensembl
chr10:98952938..98953006hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3220319, nsv3229535
SamplesNA19238, NA19240
Known GenesARHGAP19-SLIT1
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)dgv1018n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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