A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097283



Internal ID21291957
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 StatusS
Merged Variantsnsv3117200
Supporting Variants
Samplessample81
Known GenesPAM
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097283
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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