A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9817n152



Internal ID22825520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135534367..135534428hg38UCSC Ensembl
chr9:138426213..138426274hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3224204, nsv3211176
SamplesNA19238, NA19239, NA19240
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)dgv9817n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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