A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv172n145



Internal ID22813188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92846847..92850869hg38UCSC Ensembl
chr10:94606604..94610626hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg384023
hg194023
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3113060, nsv3116647
Samplessample289, sample224
Known GenesEXOC6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv172n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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