A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1236n145



Internal ID22814252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:68703704..68707731hg38UCSC Ensembl
chr9:71318620..71322647hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg384028
hg194028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3113796, nsv3114320
Samplessample349, sample348
Known GenesPIP5K1B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1236n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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