A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9626n152



Internal ID22825329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83357214..83357278hg38UCSC Ensembl
chr9:85972129..85972193hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3286722, nsv3528510, nsv3283407
SamplesHG00512, NA19238, NA19240, HG00514
Known GenesFRMD3
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)dgv9626n152
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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