A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117700



Internal ID21300966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:94838970..94846137hg38UCSC Ensembl
Innerchr15:95382199..95389366hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg387168
hg197168
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv414n145
Supporting Variantsnssv14096052
Samplessample81
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117700
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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