A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115287



Internal ID21298553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:119585531..120043637hg38UCSC Ensembl
Innerchr5:118921226..119379332hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38458107
hg19458107
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096679
Samplessample6
Known GenesFAM170A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115287
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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