A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111108



Internal ID21294374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:90855608..90861985hg38UCSC Ensembl
Innerchr10:92615365..92621742hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg386378
hg196378
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv171n145
Supporting Variantsnssv14088694
Samplessample263
Known GenesHTR7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111108
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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