A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv171n145



Internal ID22813187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:90855223..90861985hg38UCSC Ensembl
chr10:92614980..92621742hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg386763
hg196763
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3111108, nsv3115283, nsv3113625
Samplessample306, sample263, sample273
Known GenesHTR7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv171n145
Frequency
Sample Size467
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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