A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117200



Internal ID21300466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:102940541..102946076hg38UCSC Ensembl
Innerchr5:102276245..102281780hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg385536
hg195536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097283
Samplessample81
Known GenesPAM
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117200
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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