A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1237n145



Internal ID22814253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69840226..69846171hg38UCSC Ensembl
chr9:72455142..72461087hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg385946
hg195946
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3114805, nsv3115799, nsv3117406, nsv3117468
Samplessample313, sample329, sample101, sample15, sample216, sample276, sample124
Known GenesC9orf135
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1237n145
Frequency
Sample Size467
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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