A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9729n152



Internal ID22825432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:116289114..116289221hg38UCSC Ensembl
chr9:119051393..119051500hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3527678, nsv3286354, nsv3215051
SamplesHG00512, NA19238, NA19239, NA19240, HG00733, HG00513, HG00514
Known GenesPAPPA
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)dgv9729n152
Frequency
Sample Size9
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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