A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116647



Internal ID21299913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:92847323..92850869hg38UCSC Ensembl
Innerchr10:94607080..94610626hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg383547
hg193547
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv172n145
Supporting Variantsnssv14088611
Samplessample224
Known GenesEXOC6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116647
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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