A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115693



Internal ID21298959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:116669171..116675574hg38UCSC Ensembl
Innerchr7:116309225..116315628hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg386404
hg196404
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14083303
Samplessample81
Known GenesMET
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115693
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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